Canonical Allele Identifier: PA2830232921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Glu10784Asp
CA1992749
NM_133437.4:c.32352A>C
CA349500202
NM_133437.4:c.32352A>T