Canonical Allele Identifier: PA2829651113
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.His214Leu
CA2490409
NM_006722.2:c.641A>T