Allele Registry

Canonical Allele Identifier: PA2825380849

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008022

ClinVar Variation:

7584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001032626.1:p.Asn169His	CA118905 NM_001037537.2:c.505A>C