Canonical Allele Identifier: PA310561
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile24089Val
CA310560
NM_001256850.1:c.72265A>G