Canonical Allele Identifier: PA2830212806
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn3897Ser
CA311737
NM_133432.3:c.11690A>G