ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA347446
Gene: PEPD
HGNC
NCBI
Linked Data
ClinVar Variation Id:
209997
ClinVar RCV Id:
RCV000195145
RCV002517036
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000276.2:p.Ala212Pro
CA347445
NM_000285.4:c.634G>C