Canonical Allele Identifier: PA2830192110
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu4132Met
CA2002086
NM_133378.4:c.12394C>A