ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826016977
Gene: PEPD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1391035
ClinVar RCV Id:
RCV001891290
RCV002553596
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001159528.1:p.Val414Ile
CA9363878
NM_001166056.2:c.1240G>A