Canonical Allele Identifier: PA2829429696
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg694Ser
CA2005875
NM_003319.4:c.2080C>A