Canonical Allele Identifier: PA645412082
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg31242Cys
CA1987257
NM_001267550.2:c.93724C>T