Canonical Allele Identifier: PA2826413448
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179252
ClinVar RCV Id: RCV000156039 RCV001128995 RCV001131670 RCV001131667 RCV001131668 RCV001131669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr6736Pro
CA184055
NM_001256850.1:c.20206A>C