Canonical Allele Identifier: PA891853106
Gene: MPV17L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 585039
ClinVar RCV Id: RCV000709789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116072.2:p.Arg11His
CA9307564
NM_032683.3:c.32G>A