Allele Registry

Canonical Allele Identifier: PA2499294860

Gene: CASP7 HGNC NCBI

ClinVar RCV:

RCV001641928

ClinVar Variation:

1246573

HGVS (amino-acid)	Matching Registered Transcripts
NP_203126.1:p.Thr244Ser	CA5696501 NM_033340.4:c.731C>G CA378425953 NM_033340.4:c.730A>T