Canonical Allele Identifier: PA140939
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47416
ClinVar RCV Id: RCV000040686 RCV000267329 RCV000327142 RCV000363058 RCV000362027 RCV000302688 RCV000724925 RCV001427304 RCV001798184 RCV002345320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala25923Val
CA140936
NM_001256850.1:c.77768C>T