Canonical Allele Identifier: PA112806
Gene: SLC20A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29795
ClinVar RCV Id: RCV000172921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244109.1:p.Ser601Leu
CA346850
NM_001257180.2:c.1802C>T