Canonical Allele Identifier: PA2826412605
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn4997Asp
CA2002128
NM_001256850.1:c.14989A>G