Allele Registry

Canonical Allele Identifier: PA2826488981

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001253987.1:p.Asp230Glu	CA5696501 NM_001267058.2:c.690C>G CA378425959 NM_001267058.2:c.690C>A