Canonical Allele Identifier: PA2829431868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47843
ClinVar RCV Id: RCV000041112 RCV000172415 RCV000852920 RCV001083873 RCV001170876 RCV002381323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn4294His
CA142026
NM_003319.4:c.12880A>C