Canonical Allele Identifier: PA181099
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 177972
ClinVar RCV Id: RCV000154645 RCV000172380 RCV001131545 RCV001170862 RCV001131544 RCV001131546 RCV001083732 RCV001131542 RCV001131543 RCV004534959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile8832Val
CA181096
NM_001267550.2:c.26494A>G