Canonical Allele Identifier: PA2825670574
Gene: CA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17606
ClinVar RCV Id: RCV000019172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001122302.1:p.Arg247His
CA127304
NM_001128830.4:c.740G>A