Canonical Allele Identifier: PA645412612
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332700
ClinVar RCV Id: RCV000269466 RCV000284570 RCV000329031 RCV000378783 RCV000383573 RCV000727776 RCV001798783 RCV002379220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala33764Val
CA1985903
NM_001267550.2:c.101291C>T