Canonical Allele Identifier: PA2826114392
Gene: SLC34A3 HGNC NCBI
ClinVar RCV:
RCV000449572
ClinVar Variation:
397583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001170788.2:p.Thr425Ile
CA16609447
NM_001177317.2:c.1274C>T