Canonical Allele Identifier: PA2826280450
Gene: CA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305302
ClinVar RCV Id: RCV004151123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001206.2:p.Met110Lys
CA572963
NM_001215.4:c.329T>A