Canonical Allele Identifier: PA2828048236
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Tyr537Asn
CA008719
NM_001355216.1:c.1609T>A