Canonical Allele Identifier: PA658800905
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 299255
ClinVar RCV Id: RCV000319288 RCV000960582 RCV003930251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032626.1:p.Thr19Met
CA5412402
NM_001037537.2:c.56C>T