Allele Registry

Canonical Allele Identifier: PA2830105969

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_203124.1:p.Asp288Glu	CA5696501 NM_033338.6:c.864C>G CA378425959 NM_033338.6:c.864C>A