Canonical Allele Identifier: PA2573274597
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1479171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Tyr791Cys
CA376555872
NM_020975.6:c.2372A>G