Canonical Allele Identifier: PA916026793
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7587
ClinVar RCV Id: RCV000008025 RCV003473055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Gly206Ser
CA118907
NM_001323082.2:c.616G>A