Canonical Allele Identifier: PA645427856
Gene: CA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 324237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000708.1:p.Gln254Pro
CA8685530
NM_000717.5:c.761A>C