Canonical Allele Identifier: PA2499264433
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 1036986
ClinVar RCV Id: RCV001340066 RCV002476568
ClinVar Variation Id: 3175035
ClinVar RCV Id: RCV004474383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Met99Val
CA8532892
NM_003673.4:c.295A>G
CA2259200808
NM_003673.4:c.294_295delinsAG