Canonical Allele Identifier: PA645411204
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser26828Arg
CA10611616
NM_001267550.2:c.80484C>G
CA349588598
NM_001267550.2:c.80484C>A
CA349588607
NM_001267550.2:c.80482A>C