Canonical Allele Identifier: PA2830211047
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn1709Ser
CA238284
NM_133432.3:c.5126A>G