Canonical Allele Identifier: PA2830431571
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1208422
ClinVar Variation Id: 1687701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Gly393Arg
CA2490690
NM_198158.3:c.1177G>A
CA2490691
NM_198158.3:c.1177G>C