Canonical Allele Identifier: PA2827881982
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341535.1:p.His309Arg
CA353561659
NM_001354606.2:c.926A>G