Canonical Allele Identifier: PA645448949
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.Met62Val
CA2490366
NM_000248.4:c.184A>G