Canonical Allele Identifier: PA915984896
Gene: HPD HGNC NCBI

Linked Data

ClinVar Variation Id: 307482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002141.2:p.Arg279His
CA6839503
NM_002150.3:c.836G>A