Canonical Allele Identifier: PA2830243487
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr26497Ala
CA60953427
NM_133437.4:c.79489A>G