Canonical Allele Identifier: PA2827185432
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299253
ClinVar RCV Id: RCV000483319 RCV003243060 RCV000377458
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310009.1:p.Ala92Thr
CA5412312
NM_001323080.2:c.274G>A