Canonical Allele Identifier: PA645410753
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser22732Leu
CA1991173
NM_001267550.2:c.68195C>T