Canonical Allele Identifier: PA2829429788
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263595

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser821Gly
CA2005779
NM_003319.4:c.2461A>G