Canonical Allele Identifier: PA645409361
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 288760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln9198Glu
CA1999779
NM_001267550.2:c.27592C>G