Canonical Allele Identifier: PA279214
Gene: SLC38A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 208881
ClinVar RCV Id: RCV000201351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277053.2:p.Phe269Ser
CA279213
NM_033518.3:c.806T>C