Canonical Allele Identifier: PA2829445839
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191810
ClinVar RCV Id: RCV000172149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu26278Gly
CA237605
NM_003319.4:c.78833A>G