Canonical Allele Identifier: PA106774
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13934
ClinVar RCV Id: RCV000014959 RCV000021789 RCV002272020 RCV000566125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys620Trp
CA008105
NM_020975.6:c.1860C>G