Canonical Allele Identifier: PA2829435367
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202742
ClinVar RCV Id: RCV000184664 RCV000460043 RCV000619810 RCV001132250 RCV001132251 RCV001132248 RCV001132247 RCV001132249 RCV001532422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asn10696Ser
CA310146
NM_003319.4:c.32087A>G