Allele Registry

Canonical Allele Identifier: PA199560

Gene: HPCA HGNC NCBI

ClinVar RCV:

RCV000170353

ClinVar Variation:

190119

HGVS (amino-acid)	Matching Registered Transcripts
NP_002134.2:p.Thr71Asn	CA199559 NM_002143.3:c.212C>A