Canonical Allele Identifier: PA2825593914
Gene: HP HGNC NCBI

Linked Data

ClinVar Variation Id: 2512377
ClinVar RCV Id: RCV004288779

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119574.1:p.Pro96Gln
CA8159116
NM_001126102.3:c.287C>A