Canonical Allele Identifier: PA2830193201
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466938

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn7080Lys
CA60970448
NM_133378.4:c.21240C>A
CA349491342
NM_133378.4:c.21240C>G