Canonical Allele Identifier: PA2830215468
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala8731Val
CA178776
NM_133432.3:c.26192C>T