Canonical Allele Identifier: PA2826980146
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2224331
ClinVar RCV Id: RCV004084531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305067.1:p.Arg102Gln
CA8159123
NM_001318138.2:c.305G>A