Canonical Allele Identifier: PA282806
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46682
ClinVar RCV Id: RCV000039952 RCV000225946 RCV000249879 RCV001128990 RCV001528458 RCV001128991 RCV001128992 RCV001128993 RCV001128994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly6741Asp
CA282803
NM_001256850.1:c.20222G>A