Canonical Allele Identifier: PA237606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191810
ClinVar RCV Id: RCV000172149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32775Gly
CA237605
NM_133378.4:c.98324A>G