Canonical Allele Identifier: PA2825153567
Gene: CASR HGNC NCBI

Linked Data

ClinVar Variation Id: 1361649
ClinVar RCV Id: RCV001899781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000379.3:p.Ser875Arg
CA354160430
NM_000388.4:c.2623A>C
CA354160436
NM_000388.4:c.2625C>G
CA354160437
NM_000388.4:c.2625C>A