Canonical Allele Identifier: PA2826426951
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg31463Cys
CA1986202
NM_001256850.1:c.94387C>T