Canonical Allele Identifier: PA2830192622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys5562Asn
CA311930
NM_133378.4:c.16686A>C
CA349544764
NM_133378.4:c.16686A>T