Allele Registry

Canonical Allele Identifier: PA2827185905

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008022

ClinVar Variation:

7584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310012.1:p.Asn181His	CA118905 NM_001323083.2:c.541A>C