Canonical Allele Identifier: PA092449
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 5619
ClinVar RCV Id: RCV000005971 RCV002496276 RCV002512816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Pro334Arg
CA253539
NM_012434.5:c.1001C>G