Canonical Allele Identifier: PA312062
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203331
ClinVar RCV Id: RCV000642898 RCV001133190 RCV001133192 RCV001133194 RCV001170868 RCV001704957 RCV002227936 RCV001133191 RCV001133193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu7940Val
CA312061
NM_001256850.1:c.23818C>G