Canonical Allele Identifier: PA2825152058
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 2050086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Thr372Ala
CA2569595
NM_000388.4:c.1114A>G