Canonical Allele Identifier: PA2827185896
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1377863
ClinVar RCV Id: RCV001880875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310012.1:p.Asp166Tyr
CA376034187
NM_001323083.2:c.496G>T