Canonical Allele Identifier: PA2830234751
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn13849Ser
CA1991176
NM_133437.4:c.41546A>G