Canonical Allele Identifier: PA2830218188
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg13380Cys
CA1991397
NM_133432.3:c.40138C>T