Canonical Allele Identifier: PA2825152489
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1774428
ClinVar RCV Id: RCV004058653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Glu507Asp
CA354155279
NM_000388.4:c.1521A>C
CA354155280
NM_000388.4:c.1521A>T