Canonical Allele Identifier: PA2826424217
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1163426
ClinVar RCV Id: RCV001508467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val27125Leu
CA349544887
NM_001256850.1:c.81373G>C