Canonical Allele Identifier: PA183912
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179187
ClinVar RCV Id: RCV000155973 RCV000172667 RCV000242630 RCV001135859 RCV001085935 RCV001128852 RCV001128853 RCV001135860 RCV001135861 RCV004535005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp16118Gly
CA183909
NM_001267550.2:c.48353A>G