Canonical Allele Identifier: PA2830433390
Gene: MITF HGNC NCBI

Linked Data

ClinVar Variation Id: 432664
ClinVar RCV Id: RCV000498171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937821.2:p.His147Arg
CA353561659
NM_198178.3:c.440A>G