Canonical Allele Identifier: PA2830243561
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1014960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr26571Ala
CA349406047
NM_133437.4:c.79711A>G