Canonical Allele Identifier: PA2826151488
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 29792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Glu367Lys
CA128649
NM_001184967.2:c.1099G>A