Canonical Allele Identifier: PA095283
Gene: CA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 916
ClinVar RCV Id: RCV000000964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000058.1:p.His107Tyr
CA114625
NM_000067.3:c.319C>T