Canonical Allele Identifier: PA229139
Gene: SLC20A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 100856
ClinVar RCV Id: RCV000087218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006740.1:p.Ile118Thr
CA229138
NM_006749.5:c.353T>C