Canonical Allele Identifier: PA2825153692
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 2086694
ClinVar RCV Id: RCV003015549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Thr909Ser
CA82749192
NM_000388.4:c.2726C>G
CA354160629
NM_000388.4:c.2725A>T