Canonical Allele Identifier: PA658667693
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val29416Phe
CA1988182
NM_001267550.2:c.88246G>T