Canonical Allele Identifier: PA311125
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32097His
CA311124
NM_001256850.1:c.96290G>A