Canonical Allele Identifier: PA310189
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg18854His
CA310188
NM_001256850.1:c.56561G>A