Canonical Allele Identifier: PA141625
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys34293Glu
CA141622
NM_001267550.2:c.102877A>G