Canonical Allele Identifier: PA2829651191
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1305042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Leu274Ile
CA77001741
NM_006722.2:c.820C>A