Canonical Allele Identifier: PA2826151515
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1692270
ClinVar RCV Id: RCV002255873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Thr396Ile
CA353559686
NM_001184967.2:c.1187C>T