Canonical Allele Identifier: PA2580160146
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 2086694
ClinVar RCV Id: RCV003015549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Thr919Ser
CA82749192
NM_001178065.2:c.2756C>G
CA354160629
NM_001178065.2:c.2755A>T