ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826016874
Gene: PEPD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
343225
ClinVar RCV:
RCV000300960
RCV001850752
RCV002521206
ClinVar Variation:
328802
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001159528.1:p.Gly308Ser
CA9364023
NM_001166056.2:c.922G>A