Canonical Allele Identifier: PA2827882334
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 900358

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341536.1:p.Asn270Lys
CA353561440
NM_001354607.2:c.810C>A
CA353561441
NM_001354607.2:c.810C>G