Canonical Allele Identifier: PA2580173047
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1734810
ClinVar RCV Id: RCV002363878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser21661Gly
CA349435959
NM_001267550.2:c.64981A>G