Canonical Allele Identifier: PA915975803
Gene: SLC34A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5717
ClinVar RCV Id: RCV000006071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006415.3:p.Gly106Arg
CA117705
NM_006424.3:c.316G>C
CA2879413
NM_006424.3:c.316G>A