Canonical Allele Identifier: PA2830243635
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47709
ClinVar Variation Id: 915801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu26654Val
CA141752
NM_133437.4:c.79961A>T
CA60950864
NM_133437.4:c.79959_79961delinsAGT