Canonical Allele Identifier: PA2826151379
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2925353
ClinVar RCV Id: RCV003781007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Lys255Gln
CA353561631
NM_001184967.2:c.763A>C