Canonical Allele Identifier: PA2830236832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val17426Asp
CA178490
NM_133437.4:c.52277T>A