Canonical Allele Identifier: PA2828048246
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2735392
ClinVar RCV Id: RCV003531557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ser541Arg
CA376555913
NM_001355216.1:c.1621A>C
CA376555923
NM_001355216.1:c.1623C>A
CA376555925
NM_001355216.1:c.1623C>G