Canonical Allele Identifier: PA2826426396
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405089

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp30588Asn
CA1986725
NM_001256850.1:c.91762G>A