Canonical Allele Identifier: PA2826425341
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile28986Val
CA185748
NM_001256850.1:c.86956A>G