Canonical Allele Identifier: PA916066949
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val9606Ile
CA1993445
NM_133437.4:c.28816G>A