Canonical Allele Identifier: PA111543
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 44710
ClinVar RCV Id: RCV000170302 RCV000037797 RCV000765349 RCV000766898 RCV001087199 RCV002336134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Arg153His
CA134926
NM_003673.4:c.458G>A