Canonical Allele Identifier: PA284192
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47611
ClinVar RCV Id: RCV000040880 RCV000226010 RCV000246674 RCV001080938 RCV001132107 RCV001129391 RCV001132108 RCV001132109 RCV001132110 RCV001170523
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser31370Thr
CA284189
NM_001256850.1:c.94108T>A