Canonical Allele Identifier: PA916026802
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299244
ClinVar RCV Id: RCV000314971 RCV000883928 RCV003950006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310011.1:p.Arg329Gln
CA5412178
NM_001323082.2:c.986G>A