Canonical Allele Identifier: PA310494
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn23128Asp
CA310493
NM_001256850.1:c.69382A>G