Canonical Allele Identifier: PA916026792
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299250
ClinVar RCV Id: RCV002520543 RCV000430932 RCV000359852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Asn204Lys
CA5412302
NM_001323082.2:c.612C>A
CA376035402
NM_001323082.2:c.612C>G