Canonical Allele Identifier: PA2826411139
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332951
ClinVar RCV Id: RCV000312966 RCV000367691 RCV000348061 RCV000402905 RCV000404788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu2173Val
CA2005016
NM_001256850.1:c.6517T>G