Canonical Allele Identifier: PA2580375949
Gene: TNFRSF13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2325679
ClinVar RCV Id: RCV002939507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036584.1:p.Arg8Lys
CA398520653
NM_012452.3:c.23G>A