Canonical Allele Identifier: PA2829444152
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47633
ClinVar RCV Id: RCV000040902 RCV000118798 RCV000251517 RCV000299708 RCV000334610 RCV000404458 RCV000349947 RCV000407040 RCV001083282 RCV000852781 RCV001170520 RCV003993771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg24673Cys
CA231615
NM_003319.4:c.74017C>T