Canonical Allele Identifier: PA645500501
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 282451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Arg33Trp
CA8532833
NM_003673.4:c.97C>T