Allele Registry

Canonical Allele Identifier: PA111587

Gene: TCAP HGNC NCBI

ClinVar RCV:

RCV000170301

ClinVar Variation:

189787

HGVS (amino-acid)	Matching Registered Transcripts
NP_003664.1:p.Thr137Ile	CA274680 NM_003673.4:c.410C>T