Canonical Allele Identifier: PA311739
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn4135Ser
CA311737
NM_001267550.2:c.12404A>G