Allele Registry

Canonical Allele Identifier: PA2826004646

Gene: CA1 HGNC NCBI

ClinVar RCV:

RCV000019172

ClinVar Variation:

17606

HGVS (amino-acid)	Matching Registered Transcripts
NP_001158302.1:p.Arg247His	CA127304 NM_001164830.2:c.740G>A