Canonical Allele Identifier: PA2829651258
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2949784
ClinVar RCV Id: RCV003804950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Leu327Pro
CA353561791
NM_006722.2:c.980T>C