Canonical Allele Identifier: PA2830239077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47489

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg20936Gln
CA141163
NM_133437.4:c.62807G>A