Canonical Allele Identifier: PA308837
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 202108
ClinVar RCV Id: RCV000487833 RCV000560917 RCV000660576 RCV000991354 RCV001797668 RCV002453666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Cys38Phe
CA308835
NM_003673.4:c.113G>T