Canonical Allele Identifier: PA134922
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 44707
ClinVar RCV Id: RCV000037794 RCV000172590 RCV000584787 RCV000617480 RCV000989845 RCV001081397 RCV001170354 RCV003318344
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Glu13del
CA134920
NM_003673.4:c.37_39del