Canonical Allele Identifier: PA2826428818
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180582

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser33531del
CA346775
NM_001256850.1:c.100591_100593del