Canonical Allele Identifier: PA2827881611
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2925353
ClinVar RCV Id: RCV003781007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Lys312Gln
CA353561631
NM_001354605.2:c.934A>C