Canonical Allele Identifier: PA302921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp30438Asn
CA302919
NM_001256850.1:c.91312G>A