Allele Registry

Canonical Allele Identifier: PA2826980145

Gene: HP HGNC NCBI

ClinVar RCV:

RCV000017244

ClinVar Variation:

15898

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305067.1:p.Lys72Glu	CA126027 NM_001318138.2:c.214A>G