Canonical Allele Identifier: PA2830433704
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.Ser335Cys
CA353559992
NM_198178.3:c.1004C>G