Canonical Allele Identifier: PA311946
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203293
ClinVar RCV Id: RCV000329170 RCV001086431 RCV002222434 RCV000724998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys6684Arg
CA311945
NM_001256850.1:c.20051A>G