Canonical Allele Identifier: PA645408939
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser5451Gly
CA2002044
NM_001267550.2:c.16351A>G