Canonical Allele Identifier: PA2826690473
Gene: SLC9A3 HGNC NCBI
ClinVar RCV:
RCV001973501
ClinVar Variation:
1474601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271280.1:p.Gly787Arg
CA359023160
NM_001284351.3:c.2359G>C