Canonical Allele Identifier: PA2825782331
Gene: SLC12A5 HGNC NCBI
ClinVar RCV:
RCV003016373
ClinVar Variation:
2096809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128243.1:p.Met120Leu
CA409187486
NM_001134771.2:c.358A>C
CA409187488
NM_001134771.2:c.358A>T