Canonical Allele Identifier: PA2826419389
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2429551
ClinVar RCV Id: RCV003127005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro18562Ser
CA1992470
NM_001256850.1:c.55684C>T