Canonical Allele Identifier: PA2826418152
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu16240Val
CA1993760
NM_001256850.1:c.48718C>G