Canonical Allele Identifier: PA645489720
Gene: TNFRSF13C HGNC NCBI

Linked Data

ClinVar Variation Id: 341883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443177.1:p.Pro21Arg
CA10262524
NM_052945.4:c.62C>G