Canonical Allele Identifier: PA2827185450
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_001310009.1:p.Gly104Ser
CA118907
NM_001323080.2:c.310G>A