Canonical Allele Identifier: PA645412626
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33941Thr
CA1985835
NM_001267550.2:c.101822G>C