Canonical Allele Identifier: PA311020
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30838Ser
CA311019
NM_001256850.1:c.92512C>A