Canonical Allele Identifier: PA2829651374
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Ser398Pro
CA123838
NM_006722.2:c.1192T>C