Canonical Allele Identifier: PA311059
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203040
ClinVar RCV Id: RCV000468025 RCV001132340 RCV001133261 RCV001133262 RCV000727860 RCV001132339 RCV001132341 RCV002362970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg31228Cys
CA311058
NM_001256850.1:c.93682C>T