Canonical Allele Identifier: PA2827881792
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 1722868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Pro497Leu
CA353559958
NM_001354605.2:c.1490C>T