Canonical Allele Identifier: PA2829445477
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser25920Gly
CA311199
NM_003319.4:c.77758A>G