Canonical Allele Identifier: PA645410276
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr18772Ala
CA16610408
NM_001267550.2:c.56314A>G