Canonical Allele Identifier: PA891860911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 586862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35463Ala
CA1985112
NM_001267550.2:c.106388G>C