Canonical Allele Identifier: PA178080
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 165335
ClinVar RCV Id: RCV000151968 RCV001345815 RCV001753538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Ala101Thr
CA178078
NM_003673.4:c.301G>A