Canonical Allele Identifier: PA2829651546
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2941566
ClinVar RCV Id: RCV003802588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Ser497Cys
CA353559992
NM_006722.2:c.1490C>G