Canonical Allele Identifier: PA2826114177
Gene: SLC34A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 64502
ClinVar RCV Id: RCV000054689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001170788.2:p.Pro158Ser
CA216289
NM_001177317.2:c.472C>T