Canonical Allele Identifier: PA2827185903
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1964570
ClinVar RCV Id: RCV002721457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310012.1:p.Gly177Arg
CA203276251
NM_001323083.2:c.529G>A
CA376034113
NM_001323083.2:c.529G>C