Canonical Allele Identifier: PA2827882838
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1721237
ClinVar RCV Id: RCV002294918

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Thr405Ile
CA353559741
NM_001354608.2:c.1214C>T