Canonical Allele Identifier: PA645412965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 389846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile35947Ser
CA16604078
NM_001267550.2:c.107840T>G