Canonical Allele Identifier: PA2826410011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr300Asn
CA2006201
NM_001256850.1:c.899C>A