Canonical Allele Identifier: PA2826427351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys32079Arg
CA178375
NM_001256850.1:c.96236A>G