Canonical Allele Identifier: PA2827882442
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 346497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Pro385Ala
CA2490626
NM_001354607.2:c.1153C>G