Canonical Allele Identifier: PA645409235
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly8053Ser
CA2000493
NM_001267550.2:c.24157G>A