Allele Registry

Canonical Allele Identifier: PA2826488952

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_001253985.1:p.Asp255Glu	CA5696501 NM_001267056.2:c.765C>G CA378425959 NM_001267056.2:c.765C>A