Canonical Allele Identifier: PA2827185491
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1922339
ClinVar RCV Id: RCV002621584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310009.1:p.Arg145Trp
CA5412247
NM_001323080.2:c.433C>T