Canonical Allele Identifier: PA915992788
Gene: TCAP HGNC NCBI

Linked Data

ClinVar Variation Id: 811127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003664.1:p.Asp129Gly
CA399305473
NM_003673.4:c.386A>G