Canonical Allele Identifier: PA311569
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203172
ClinVar RCV Id: RCV000642866 RCV001704948 RCV002372139 RCV003150078 RCV003330548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys3284Arg
CA311567
NM_001256850.1:c.9851A>G