Canonical Allele Identifier: PA645408928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Leu5376Met
CA2002086
NM_001267550.2:c.16126C>A