Canonical Allele Identifier: PA915994589
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 426474
ClinVar RCV Id: RCV000489392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171536.2:p.Val141Ala
CA354362868
NM_001178065.2:c.422T>C