Canonical Allele Identifier: PA2827882861
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1979759
ClinVar RCV Id: RCV002756107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Met428Val
CA2490671
NM_001354608.2:c.1282A>G