Canonical Allele Identifier: PA1139687050
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 851369
ClinVar RCV Id: RCV001055752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35352Cys
CA60953460
NM_001267550.2:c.106055C>G