Canonical Allele Identifier: PA2826423234
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Tyr25412Asn
CA1989244
NM_001256850.1:c.76234T>A