Canonical Allele Identifier: PA2826426297
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 498721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30417Trp
CA1986809
NM_001256850.1:c.91249C>T