Canonical Allele Identifier: PA916065541
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 288762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile6381Phe
CA1995375
NM_133437.4:c.19141A>T