Canonical Allele Identifier: PA2827081418
Gene: CA8 HGNC NCBI

Linked Data

ClinVar Variation Id: 17604
ClinVar RCV Id: RCV000019170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308766.1:p.Ser100Pro
CA127301
NM_001321837.1:c.298T>C