Canonical Allele Identifier: PA2826151634
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171897.1:p.Met62Val
CA2490366
NM_001184968.2:c.184A>G