Canonical Allele Identifier: PA2830431510
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1305242
ClinVar RCV Id: RCV001768449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Gly351Val
CA353559748
NM_198158.3:c.1052G>T