Canonical Allele Identifier: PA2826429160
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val33894Ala
CA1985065
NM_001256850.1:c.101681T>C