Canonical Allele Identifier: PA2829584869
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2267717
ClinVar RCV Id: RCV004119138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005134.1:p.Pro155Arg
CA8159117
NM_005143.5:c.464C>G