Canonical Allele Identifier: PA1139687291
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 863553
ClinVar RCV Id: RCV001070546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35444Ser
CA349406040
NM_001267550.2:c.106331C>G
CA349406045
NM_001267550.2:c.106330A>T