Canonical Allele Identifier: PA915994542
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 237767
ClinVar RCV Id: RCV000226572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Phe98Leu
CA10582119
NM_001178065.2:c.294T>G
CA354362577
NM_001178065.2:c.292T>C
CA354362582
NM_001178065.2:c.294T>A