Canonical Allele Identifier: PA178377
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys33720Arg
CA178375
NM_001267550.2:c.101159A>G