Canonical Allele Identifier: PA2826434779
Gene: SLC20A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 363080
ClinVar RCV Id: RCV000372995 RCV001580040 RCV001522227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244110.1:p.Gly304Ser
CA4733435
NM_001257181.2:c.910G>A