Canonical Allele Identifier: PA2830214659
Gene: TTN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile7318Val
CA349608043
NM_133432.3:c.21952A>G