Canonical Allele Identifier: PA2826690430
Gene: SLC9A3 HGNC NCBI
ClinVar RCV:
RCV002303360
ClinVar Variation:
1716282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271280.1:p.Leu708Arg
CA359024213
NM_001284351.3:c.2123T>G