Canonical Allele Identifier: PA284167
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47600
ClinVar RCV Id: RCV000040869 RCV000419770 RCV000768846 RCV000621374 RCV001129725 RCV000852783 RCV001132433 RCV001082901 RCV001129726 RCV001132434 RCV001132435
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn31156Ser
CA284164
NM_001256850.1:c.93467A>G