Canonical Allele Identifier: PA2826423306
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile25541Asn
CA1989192
NM_001256850.1:c.76622T>A