Canonical Allele Identifier: PA110353
Gene: CA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 17608
ClinVar RCV Id: RCV000019174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000708.1:p.Arg219Ser
CA258045
NM_000717.5:c.655C>A