Canonical Allele Identifier: PA2826151358
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2047039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Pro221Ala
CA2490481
NM_001184967.2:c.661C>G