Canonical Allele Identifier: PA2825152157
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1368152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Ala390Asp
CA354152739
NM_000388.4:c.1169C>A