Canonical Allele Identifier: PA2826016981
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_001159528.1:p.Ser419Arg
CA405219699
NM_001166056.2:c.1257C>G
CA405219700
NM_001166056.2:c.1257C>A
CA405219706
NM_001166056.2:c.1255A>C