Canonical Allele Identifier: PA2830431891
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2949784
ClinVar RCV Id: RCV003804950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Leu328Pro
CA353561791
NM_198159.3:c.983T>C