Canonical Allele Identifier: PA645510245
Gene: TNFRSF13C HGNC NCBI

Linked Data

ClinVar Variation Id: 440343
ClinVar Variation Id: 471473
ClinVar RCV Id: RCV000538153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443177.1:p.Gly64Val
CA10262514
NM_052945.4:c.191G>T
CA658658924
NM_052945.4:c.191_192delinsTT