Canonical Allele Identifier: PA2830431406
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 506003
ClinVar RCV Id: RCV000604068

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Ala288Val
CA353559351
NM_198158.3:c.863C>T