Canonical Allele Identifier: PA2827081440
Gene: CA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 29620
ClinVar RCV Id: RCV000022460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308766.1:p.Arg237Gln
CA128507
NM_001321837.1:c.710G>A