ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827186067
Gene: PHYH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
22627
ClinVar RCV:
RCV000008026
RCV001851728
RCV003473056
ClinVar Variation:
7588
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001310013.1:p.Arg177Gln
CA118908
NM_001323084.2:c.530G>A