Canonical Allele Identifier: PA2826429026
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1906541
ClinVar RCV Id: RCV002586988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys33752Asn
CA349406755
NM_001256850.1:c.101256G>T
CA349406757
NM_001256850.1:c.101256G>C