Allele Registry

Canonical Allele Identifier: PA2827081418

Gene: CA8 HGNC NCBI

ClinVar RCV:

RCV000019170

ClinVar Variation:

17604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308766.1:p.Ser100Pro	CA127301 NM_001321837.1:c.298T>C