Canonical Allele Identifier: PA2826017320
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1918310
ClinVar RCV Id: RCV002617237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Ser396Arg
CA405219699
NM_001166057.2:c.1188C>G
CA405219700
NM_001166057.2:c.1188C>A
CA405219706
NM_001166057.2:c.1186A>C