Canonical Allele Identifier: PA2829651541
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2077794
ClinVar RCV Id: RCV002993493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Ser494Phe
CA353559976
NM_006722.2:c.1481C>T