Canonical Allele Identifier: PA645411917
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala29975Val
CA1987854
NM_001267550.2:c.89924C>T