Canonical Allele Identifier: PA2830243931
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser26966Arg
CA311295
NM_133437.4:c.80898T>G
CA349400210
NM_133437.4:c.80898T>A
CA349400215
NM_133437.4:c.80896A>C