Canonical Allele Identifier: PA2826427039
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2581847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile31580Val
CA60961649
NM_001256850.1:c.94738A>G