Canonical Allele Identifier: PA2826422189
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp23523Asn
CA1990042
NM_001256850.1:c.70567G>A