Allele Registry

Canonical Allele Identifier: PA126031

Gene: HP HGNC NCBI

ClinVar RCV:

RCV000017244

ClinVar Variation:

15898

HGVS (amino-acid)	Matching Registered Transcripts
NP_005134.1:p.Lys72Glu	CA126027 NM_005143.5:c.214A>G