Canonical Allele Identifier: PA2826016975
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_001159528.1:p.Glu412Asp
CA9363881
NM_001166056.2:c.1236G>C
CA405219741
NM_001166056.2:c.1236G>T