Canonical Allele Identifier: PA2741882254
Gene: SLC12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2606264
ClinVar RCV Id: RCV003369129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371065.1:p.Val272Ala
CA7546907
NM_001384136.1:c.815T>C