Canonical Allele Identifier: PA2825380853
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7580
ClinVar RCV Id: RCV000008018 RCV000255609 RCV000505105 RCV000665657 RCV002426496
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032626.1:p.Arg175Trp
CA118904
NM_001037537.2:c.523C>T