Canonical Allele Identifier: PA110342
Gene: CA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 17607
ClinVar RCV Id: RCV000019173 RCV000336591 RCV001247433 RCV003914854
JSON-LD

Amino-acid Alleles

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