Canonical Allele Identifier: PA2826418232
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp16398Asn
CA1993694
NM_001256850.1:c.49192G>A