Canonical Allele Identifier: PA2827186038
Gene: PHYH HGNC NCBI

Linked Data

ClinVar Variation Id: 631628
ClinVar RCV Id: RCV000778275 RCV002535632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310013.1:p.Gly137Arg
CA5412252
NM_001323084.2:c.409G>A
CA376034433
NM_001323084.2:c.409G>C