Canonical Allele Identifier: PA2830226945
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405037
ClinVar RCV Id: RCV000476896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Gly26226Val
CA16610295
NM_133432.3:c.78677G>T