Canonical Allele Identifier: PA2826417088
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg14257Gln
CA1995005
NM_001256850.1:c.42770G>A