Allele Registry

Canonical Allele Identifier: PA110342

Gene: CA4 HGNC NCBI

ClinVar RCV:

RCV000019173

RCV000336591

RCV001247433

RCV003914854

ClinVar Variation:

17607

HGVS (amino-acid)	Matching Registered Transcripts
NP_000708.1:p.Arg14Trp	CA258044 NM_000717.5:c.40C>T