Canonical Allele Identifier: PA309598
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr10481Ala
CA309596
NM_001267550.2:c.31441A>G