Canonical Allele Identifier: PA123841
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 14277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Ser399Pro
CA123838
NM_198159.3:c.1195T>C