Canonical Allele Identifier: PA2827186067
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7588
ClinVar RCV Id: RCV000008026 RCV001851728 RCV003473056
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310013.1:p.Arg177Gln
CA118908
NM_001323084.2:c.530G>A