Canonical Allele Identifier: PA2826429443
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser34214Ile
CA60949238
NM_001256850.1:c.102641G>T