Canonical Allele Identifier: PA2573221120
Gene: CA5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1495000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001730.1:p.Val172Leu
CA8223446
NM_001739.2:c.514G>T
CA397041803
NM_001739.2:c.514G>C