Canonical Allele Identifier: PA2826980158
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2345586
ClinVar RCV Id: RCV004182001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305067.1:p.Arg218His
CA8159198
NM_001318138.2:c.653G>A