Canonical Allele Identifier: PA916026799
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7588
ClinVar RCV Id: RCV000008026 RCV001851728 RCV003473056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Arg277Gln
CA118908
NM_001323082.2:c.830G>A