Canonical Allele Identifier: PA308822
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 202103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Ala97Val
CA308820
NM_003673.4:c.290C>T