Canonical Allele Identifier: PA2826410697
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala1384Ser
CA2005396
NM_001256850.1:c.4150G>T