Canonical Allele Identifier: PA2827881726
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1975262
ClinVar RCV Id: RCV002755585
ClinVar Variation Id: 2580780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Asn429Lys
CA353559531
NM_001354605.2:c.1287C>A
CA353559532
NM_001354605.2:c.1287C>G