Canonical Allele Identifier: PA237819
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191899
ClinVar RCV Id: RCV000172260 RCV001083382 RCV001132951 RCV001132000 RCV001132001 RCV001132002 RCV001132003 RCV002281995 RCV002336413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg21700His
CA237818
NM_133378.4:c.65099G>A