Canonical Allele Identifier: PA2830200929
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala26427Thr
CA1988398
NM_133378.4:c.79279G>A