Allele Registry

Canonical Allele Identifier: PA2826281145

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001218.1:p.Asp255Glu	CA5696501 NM_001227.5:c.765C>G CA378425959 NM_001227.5:c.765C>A