Canonical Allele Identifier: PA2826428975
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191810
ClinVar RCV Id: RCV000172149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu33702Gly
CA237605
NM_001256850.1:c.101105A>G