Canonical Allele Identifier: PA2827881793
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1716465
ClinVar RCV Id: RCV002303514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Pro497Ala
CA353559954
NM_001354605.2:c.1489C>G