Canonical Allele Identifier: PA139166
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46771
ClinVar RCV Id: RCV000040041 RCV000118746 RCV000249830 RCV000268699 RCV000293596 RCV000327425 RCV000333139 RCV000382034 RCV000852887 RCV000769050 RCV001083462 RCV004528204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val8660Ile
CA139162
NM_001267550.2:c.25978G>A