Canonical Allele Identifier: PA108303
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 7587
ClinVar RCV Id: RCV000008025 RCV003473055
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006205.1:p.Gly204Ser
CA118907
NM_006214.4:c.610G>A