Canonical Allele Identifier: PA2826131008
Gene: SLC34A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5717
ClinVar RCV Id: RCV000006071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171470.2:p.Gly105Arg
CA117705
NM_001177999.2:c.313G>C
CA2879413
NM_001177999.2:c.313G>A