Canonical Allele Identifier: PA2580178104
Gene: CA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2305302
ClinVar RCV Id: RCV004151123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257430.1:p.Met50Lys
CA572963
NM_001270501.2:c.149T>A