Allele Registry

Canonical Allele Identifier: PA2827185375

Gene: PHYH HGNC NCBI

ClinVar Variation Id: 299255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310009.1:p.Thr19Met	CA5412402 NM_001323080.2:c.56C>T