Canonical Allele Identifier: PA916060957
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile9305Val
CA1998891
NM_133378.4:c.27913A>G