Canonical Allele Identifier: PA915964732
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 640675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Ser997Tyr
CA354161216
NM_000388.4:c.2990C>A