Canonical Allele Identifier: PA2828910029
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157871
ClinVar RCV Id: RCV003078317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369561.1:p.Ala169Pro
CA364717883
NM_001382632.1:c.505G>C