Canonical Allele Identifier: PA2827881706
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Pro407Ala
CA2490626
NM_001354605.2:c.1219C>G