Canonical Allele Identifier: PA915995570
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 8349
ClinVar Variation Id: 1106072
ClinVar RCV Id: RCV001430695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Ala996Ser
CA119531
NM_001178065.2:c.2986G>T
CA2499216416
NM_001178065.2:c.2985_2986delinsTT