Canonical Allele Identifier: PA128356
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24939
ClinVar RCV Id: RCV000409436 RCV000411890 RCV000566113 RCV000457504 RCV000764900 RCV001818174 RCV003466868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Tyr791Asn
CA008719
NM_020630.6:c.2371T>A