Canonical Allele Identifier: PA2830240403
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132138
ClinVar RCV Id: RCV000119026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn22913Lys
CA358830
NM_133437.4:c.68739C>G
CA349462615
NM_133437.4:c.68739C>A