Canonical Allele Identifier: PA645410985
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp24850Gly
CA1990181
NM_001267550.2:c.74549A>G