ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA107643
Gene: PEPD
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
15250
ClinVar RCV:
RCV000000235
RCV003555875
ClinVar Variation:
211
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000276.2:p.Arg184Gln
CA214913
NM_000285.4:c.551G>A