Canonical Allele Identifier: PA658817376
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 512644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala35378Val
CA1985159
NM_001267550.2:c.106133C>T