Canonical Allele Identifier: PA645410871
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile23719Val
CA1990671
NM_001267550.2:c.71155A>G