Canonical Allele Identifier: PA2829641225
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 2166417
ClinVar RCV Id: RCV003091752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006205.1:p.Leu262Pro
CA376034130
NM_006214.4:c.785T>C