Canonical Allele Identifier: PA2826426850
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47609
ClinVar RCV Id: RCV000040878 RCV000864110 RCV001132222 RCV001132224 RCV001132221 RCV001132223 RCV001132220 RCV001561054 RCV003486614 RCV004541194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys31296Glu
CA141494
NM_001256850.1:c.93886A>G