Canonical Allele Identifier: PA139488
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46909
ClinVar RCV Id: RCV000040179 RCV000172679 RCV000247302 RCV000769039 RCV001081699 RCV001133178 RCV001133179 RCV001132263 RCV001132265 RCV001132264 RCV004534895
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val10321Ile
CA139486
NM_133378.4:c.30961G>A