Canonical Allele Identifier: PA140682
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47320
ClinVar RCV Id: RCV000040590 RCV000253827 RCV000264085 RCV000322850 RCV000328591 RCV000377423 RCV000383061 RCV000474900 RCV000769950 RCV001703907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr24390Ala
CA140678
NM_001267550.2:c.73168A>G