Canonical Allele Identifier: PA2825380840
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_001032626.1:p.Asp154Tyr
CA376034187
NM_001037537.2:c.460G>T