Canonical Allele Identifier: PA2826414735
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser9293Asn
CA1999512
NM_001256850.1:c.27878G>A