Canonical Allele Identifier: PA2826521104
Gene: CA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2359996
ClinVar RCV Id: RCV004198810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257429.1:p.His113Tyr
CA572964
NM_001270500.2:c.337C>T