Canonical Allele Identifier: PA2829584868
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2512377
ClinVar RCV Id: RCV004288779
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005134.1:p.Pro155Gln
CA8159116
NM_005143.5:c.464C>A