Canonical Allele Identifier: PA2827185901
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2166417
ClinVar RCV Id: RCV003091752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310012.1:p.Leu174Pro
CA376034130
NM_001323083.2:c.521T>C