Canonical Allele Identifier: PA2741821728
Gene: CA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2803344
ClinVar RCV Id: RCV003679469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000708.1:p.Ala6Val
CA8685177
NM_000717.5:c.17C>T