Canonical Allele Identifier: PA2826151351
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2931438
ClinVar RCV Id: RCV003785140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Gln216Arg
CA77001738
NM_001184967.2:c.647A>G