Canonical Allele Identifier: PA645433030
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_006205.1:p.Arg201Gly
CA5412303
NM_006214.4:c.601C>G