Canonical Allele Identifier: PA2826416591
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe13199Tyr
CA10611673
NM_001256850.1:c.39596T>A