Canonical Allele Identifier: PA915995913
Gene: SLC12A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 8753
ClinVar RCV Id: RCV000009296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171761.1:p.Val272Phe
CA119889
NM_001184832.2:c.814G>T