Canonical Allele Identifier: PA332891
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136102
ClinVar RCV Id: RCV000123300 RCV001762280 RCV001012544 RCV002483238 RCV000662401 RCV004542930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly548Ser
CA007695
NM_020975.6:c.1642G>A