Canonical Allele Identifier: PA2826815021
Gene: CA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17606
ClinVar RCV Id: RCV000019172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278896.1:p.Arg181His
CA127304
NM_001291967.2:c.542G>A