Canonical Allele Identifier: PA311878
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203271
ClinVar RCV Id: RCV000769071 RCV001129966 RCV001129963 RCV001129964 RCV000726445 RCV001081900 RCV001729441 RCV001129965 RCV001135006 RCV004537569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg5819Gln
CA311877
NM_001256850.1:c.17456G>A