Canonical Allele Identifier: PA310266
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp21399Asn
CA310264
NM_001267550.2:c.64195G>A