Canonical Allele Identifier: PA645448950
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.His108Leu
CA2490409
NM_000248.4:c.323A>T