Canonical Allele Identifier: PA916026791
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299251
ClinVar RCV Id: RCV000267540 RCV000487565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Arg203Gly
CA5412303
NM_001323082.2:c.607C>G