Canonical Allele Identifier: PA2830432173
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.Ser498Cys
CA353559992
NM_198159.3:c.1493C>G