Canonical Allele Identifier: PA2827185502
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1025445
ClinVar RCV Id: RCV001325758
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310009.1:p.Phe158Val
CA376034160
NM_001323080.2:c.472T>G