Canonical Allele Identifier: PA2829641219
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1025445
ClinVar RCV Id: RCV001325758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006205.1:p.Phe258Val
CA376034160
NM_006214.4:c.772T>G