Canonical Allele Identifier: PA2825105738
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1208422
ClinVar Variation Id: 1687701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Gly399Arg
CA2490690
NM_000248.4:c.1195G>A
CA2490691
NM_000248.4:c.1195G>C