Canonical Allele Identifier: PA2580160229
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1796791
ClinVar RCV Id: RCV004062408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Leu960Phe
CA354160901
NM_001178065.2:c.2878C>T