Canonical Allele Identifier: PA2825304964
Gene: SLC13A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2896827
ClinVar RCV Id: RCV003733134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001011554.1:p.Asn32Lys
CA315749328
NM_001011554.3:c.96C>A
CA409270013
NM_001011554.3:c.96C>G