Canonical Allele Identifier: PA310395
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg21747Gln
CA310394
NM_001256850.1:c.65240G>A