Canonical Allele Identifier: PA2830223881
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 284493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn22627Ser
CA10604814
NM_133432.3:c.67880A>G