Canonical Allele Identifier: PA2830202312
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516026

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn29394Asp
CA1986859
NM_133378.4:c.88180A>G