Canonical Allele Identifier: PA658664827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu6219Lys
CA2001565
NM_001267550.2:c.18655G>A