Canonical Allele Identifier: PA2580375957
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2430512
ClinVar RCV Id: RCV003129066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Arg84Ser
CA398520147
NM_012452.3:c.252G>T
CA398520148
NM_012452.3:c.252G>C