Canonical Allele Identifier: PA2830233359
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn11568Ser
CA140219
NM_133437.4:c.34703A>G