Canonical Allele Identifier: PA2829651492
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2196416
ClinVar RCV Id: RCV002651075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006713.1:p.Pro467Ser
CA2490666
NM_006722.2:c.1399C>T