Allele Registry

Canonical Allele Identifier: PA108252

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008022

ClinVar Variation:

7584

HGVS (amino-acid)	Matching Registered Transcripts
NP_006205.1:p.Asn269His	CA118905 NM_006214.4:c.805A>C