Canonical Allele Identifier: PA2826412335
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp4449Asn
CA60982481
NM_001256850.1:c.13345G>A