Allele Registry

Canonical Allele Identifier: PA2826488968

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001253986.1:p.Asp340Glu	CA5696501 NM_001267057.1:c.1020C>G CA378425959 NM_001267057.1:c.1020C>A