Canonical Allele Identifier: PA645383684
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg2501Gln
CA2004801
NM_133379.5:c.7502G>A