Canonical Allele Identifier: PA2830237447
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn18380Ser
CA310659
NM_133437.4:c.55139A>G