Allele Registry

Canonical Allele Identifier: PA2827060113

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307840.1:p.Asp263Glu	CA5696501 NM_001320911.2:c.789C>G CA378425959 NM_001320911.2:c.789C>A