Canonical Allele Identifier: PA916057477
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937801.1:p.Met62Val
CA2490366
NM_198158.3:c.184A>G