Canonical Allele Identifier: PA108249
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7580
ClinVar RCV Id: RCV000008018 RCV000255609 RCV000505105 RCV000665657 RCV002426496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006205.1:p.Arg275Trp
CA118904
NM_006214.4:c.823C>T