Canonical Allele Identifier: PA178396
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp32822Gly
CA178394
NM_001267550.2:c.98465A>G