Allele Registry

Canonical Allele Identifier: PA214567

Gene: HPCA HGNC NCBI

ClinVar RCV:

RCV000170352

ClinVar Variation:

190118

HGVS (amino-acid)	Matching Registered Transcripts
NP_002134.2:p.Asn75Lys	CA214566 NM_002143.3:c.225C>A CA339680431 NM_002143.3:c.225C>G