Canonical Allele Identifier: PA141497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys32937Glu
CA141494
NM_001267550.2:c.98809A>G