Canonical Allele Identifier: PA2827882830
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1692270
ClinVar RCV Id: RCV002255873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341537.1:p.Thr396Ile
CA353559686
NM_001354608.2:c.1187C>T