Canonical Allele Identifier: PA2830219460
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_597676.3:p.Thr15450Ala
CA140678
NM_133432.3:c.46348A>G