Canonical Allele Identifier: PA2580177327
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1761050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35370Ala
CA60953427
NM_001267550.2:c.106108A>G