Canonical Allele Identifier: PA2830239589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180070
ClinVar RCV Id: RCV000156873 RCV000727085 RCV001130618 RCV001130620 RCV001130619 RCV001130621 RCV001130622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile21754Val
CA185748
NM_133437.4:c.65260A>G