Canonical Allele Identifier: PA2826151471
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171896.1:p.Ser347Pro
CA123838
NM_001184967.2:c.1039T>C