Canonical Allele Identifier: PA2829435362
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly10685Ser
CA231599
NM_003319.4:c.32053G>A