Canonical Allele Identifier: PA2829445958
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1397267
ClinVar RCV Id: RCV001906061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile26395Val
CA349405629
NM_003319.4:c.79183A>G