Canonical Allele Identifier: PA645510386
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 440367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val9332Met
CA1999678
NM_001267550.2:c.27994G>A