Canonical Allele Identifier: PA645500495
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 263956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Arg18Trp
CA10587902
NM_003673.4:c.52C>T