Canonical Allele Identifier: PA2827186006
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_001310013.1:p.Gly106Ser
CA118907
NM_001323084.2:c.316G>A