Canonical Allele Identifier: PA2741882059
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2563375
ClinVar RCV Id: RCV003301536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369560.1:p.Ala440Val
CA364720026
NM_001382631.1:c.1319C>T