Canonical Allele Identifier: PA2830193606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 682161
ClinVar RCV Id: RCV000842177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile8135Leu
CA349440174
NM_133378.4:c.24403A>T
CA349440181
NM_133378.4:c.24403A>C