Canonical Allele Identifier: PA2829473994
Gene: TNFSF13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1181749
ClinVar RCV Id: RCV001539204 RCV003487442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003799.1:p.Gly67Arg
CA8350964
NM_003808.4:c.199G>A
CA397868518
NM_003808.4:c.199G>C