Canonical Allele Identifier: PA2827185713
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299253
ClinVar RCV Id: RCV000483319 RCV003243060 RCV000377458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Ala194Thr
CA5412312
NM_001323082.2:c.580G>A