Canonical Allele Identifier: PA2825140672
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_000276.2:p.Ser460Arg
CA405219699
NM_000285.4:c.1380C>G
CA405219700
NM_000285.4:c.1380C>A
CA405219706
NM_000285.4:c.1378A>C