Canonical Allele Identifier: PA658817387
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35504Thr
CA1985096
NM_001267550.2:c.106511G>C