Allele Registry

Canonical Allele Identifier: PA2741905097

Gene: TCAP HGNC NCBI

ClinVar RCV:

RCV003428253

ClinVar Variation:

2647721

HGVS (amino-acid)	Matching Registered Transcripts
NP_003664.1:p.Thr137Lys	CA8532907 NM_003673.4:c.410C>A