Allele Registry

Canonical Allele Identifier: PA340780

Gene: CSTB HGNC NCBI

ClinVar RCV:

RCV000008908

ClinVar Variation:

8400

HGVS (amino-acid)	Matching Registered Transcripts
NP_000091.1:p.Gln71Pro	CA340778 NM_000100.4:c.212A>C