Allele Registry

Canonical Allele Identifier: PA2827186064

Gene: PHYH HGNC NCBI

ClinVar RCV:

RCV000008022

ClinVar Variation:

7584

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310013.1:p.Asn171His	CA118905 NM_001323084.2:c.511A>C