Allele Registry

Canonical Allele Identifier: PA181035

Gene: TCAP HGNC NCBI

ClinVar RCV:

RCV000154598

RCV000232686

RCV000248260

RCV000770524

RCV001126346

RCV001126347

RCV001529978

ClinVar Variation:

177939

HGVS (amino-acid)	Matching Registered Transcripts
NP_003664.1:p.Ser11Leu	CA181033 NM_003673.4:c.32C>T