Canonical Allele Identifier: PA645409336
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp8873Glu
CA1999959
NM_001267550.2:c.26619C>A
CA349467085
NM_001267550.2:c.26619C>G