Canonical Allele Identifier: PA2830229413
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn1709Ser
CA238284
NM_133437.4:c.5126A>G