Canonical Allele Identifier: PA2828048287
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13946
ClinVar RCV Id: RCV000014973 RCV000021854 RCV000354366 RCV000487450 RCV000596480 RCV000561258
ClinVar Variation Id: 38613
ClinVar RCV Id: RCV000021853 RCV000419916 RCV000425568 RCV000426266 RCV000436948 RCV000437130 RCV000479688 RCV002453279 RCV003226171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Val550Leu
CA008758
NM_001355216.1:c.1648G>C
CA008766
NM_001355216.1:c.1648G>T