Canonical Allele Identifier: PA2830433709
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1208422
ClinVar Variation Id: 1687701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Gly337Arg
CA2490690
NM_198178.3:c.1009G>A
CA2490691
NM_198178.3:c.1009G>C