Canonical Allele Identifier: PA2826429513
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val34287Glu
CA1984876
NM_001256850.1:c.102860T>A