Canonical Allele Identifier: PA2573185690
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1349538
ClinVar RCV Id: RCV002046995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Ser272Arg
CA354151413
NM_001178065.2:c.814A>C
CA354151417
NM_001178065.2:c.816T>A
CA354151418
NM_001178065.2:c.816T>G