Canonical Allele Identifier: PA128334
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24934
ClinVar RCV Id: RCV000034769 RCV000039052 RCV000162947 RCV000340996 RCV000376859 RCV000290703 RCV000385080 RCV000660243 RCV001083339 RCV003315508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Gly691Ser
CA008562
NM_020630.6:c.2071G>A