Canonical Allele Identifier: PA2827186031
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 947644
ClinVar RCV Id: RCV001218757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310013.1:p.Gly130Ala
CA203276388
NM_001323084.2:c.389G>C