Canonical Allele Identifier: PA2827881749
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 2113893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341534.1:p.Asn458Asp
CA353559716
NM_001354605.2:c.1372A>G