Canonical Allele Identifier: PA2826412070
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 626696
ClinVar RCV Id: RCV000770110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu3930Gly
CA60984099
NM_001256850.1:c.11789A>G