Canonical Allele Identifier: PA069327
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 222831

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Gly150Ser
CA069190
NM_003673.4:c.448G>A