Canonical Allele Identifier: PA2826428447
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1481795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile33171Val
CA349411741
NM_001256850.1:c.99511A>G