Canonical Allele Identifier: PA2826412705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282833

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly5176Ser
CA2002027
NM_001256850.1:c.15526G>A