Canonical Allele Identifier: PA915982279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile9954Val
CA1999029
NM_001256850.1:c.29860A>G