Canonical Allele Identifier: PA645448951
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000239.1:p.His209Arg
CA353561659
NM_000248.4:c.626A>G