Canonical Allele Identifier: PA2826428963
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1439658
ClinVar RCV Id: RCV001958136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys33686Arg
CA349407302
NM_001256850.1:c.101057A>G