Canonical Allele Identifier: PA2826419656
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn19059Asp
CA1992270
NM_001256850.1:c.57175A>G