Canonical Allele Identifier: PA284168
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47600
ClinVar RCV Id: RCV000040869 RCV000419770 RCV000768846 RCV000621374 RCV001129725 RCV000852783 RCV001132433 RCV001082901 RCV001129726 RCV001132434 RCV001132435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn32797Ser
CA284164
NM_001267550.2:c.98390A>G