Canonical Allele Identifier: PA2826412001
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 385539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala3794Gly
CA2002731
NM_001256850.1:c.11381C>G