Canonical Allele Identifier: PA2830203984
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 534977
ClinVar RCV Id: RCV000642721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32221Gln
CA349411899
NM_133378.4:c.96661G>C