Canonical Allele Identifier: PA915994629
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 35800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Ser166Gly
CA213601
NM_001178065.2:c.496A>G