Canonical Allele Identifier: PA2830431844
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937802.1:p.His310Arg
CA353561659
NM_198159.3:c.929A>G