Canonical Allele Identifier: PA645409784
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr14501Ser
CA1995842
NM_001267550.2:c.43502C>G
CA349650320
NM_001267550.2:c.43501A>T