Canonical Allele Identifier: PA2826017314
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2154006
ClinVar RCV Id: RCV003069055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Glu389Asp
CA9363881
NM_001166057.2:c.1167G>C
CA405219741
NM_001166057.2:c.1167G>T