Canonical Allele Identifier: PA645489722
Gene: TNFRSF13C HGNC NCBI

Linked Data

ClinVar Variation Id: 341877
ClinVar RCV Id: RCV000506848 RCV000539736 RCV001197550 RCV003884501
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443177.1:p.Arg106Gln
CA10262484
NM_052945.4:c.317G>A