Canonical Allele Identifier: PA2826415838
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val11761Phe
CA1996603
NM_001256850.1:c.35281G>T