Canonical Allele Identifier: PA2580327617
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2224331
ClinVar RCV Id: RCV004084531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005134.1:p.Arg161Gln
CA8159123
NM_005143.5:c.482G>A