Canonical Allele Identifier: PA2827881781
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1308880
ClinVar RCV Id: RCV001754768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Asp487Asn
CA2490673
NM_001354605.2:c.1459G>A