Canonical Allele Identifier: PA2826521105
Gene: CA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2543077
ClinVar RCV Id: RCV004316549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257429.1:p.Val128Met
CA17706892
NM_001270500.2:c.382G>A