Canonical Allele Identifier: PA2830232984
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn10888Ser
CA310146
NM_133437.4:c.32663A>G