Canonical Allele Identifier: PA645412261
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile32009Arg
CA1986834
NM_001267550.2:c.96026T>G