Canonical Allele Identifier: PA308819
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 202102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Arg87Trp
CA308817
NM_003673.4:c.259C>T