Canonical Allele Identifier: PA2827881747
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1692270
ClinVar RCV Id: RCV002255873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Thr453Ile
CA353559686
NM_001354605.2:c.1358C>T