Allele Registry

Canonical Allele Identifier: PA101137

Gene: CST3 HGNC NCBI

ClinVar RCV:

RCV000005988

ClinVar Variation:

5634

HGVS (amino-acid)	Matching Registered Transcripts
NP_000090.1:p.Leu94Gln	CA117662 NM_000099.4:c.281T>A