Allele Registry

Canonical Allele Identifier: PA2826815030

Gene: CA1 HGNC NCBI

ClinVar RCV:

RCV000019172

ClinVar Variation:

17606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278897.1:p.Arg134His	CA127304 NM_001291968.2:c.401G>A