Canonical Allele Identifier: PA916066599
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165991
ClinVar RCV Id: RCV000152325 RCV000727183 RCV001087840 RCV001170609 RCV002453499 RCV004544372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Met8812Ile
CA178772
NM_133437.4:c.26436G>A
CA349568595
NM_133437.4:c.26436G>T
CA349568596
NM_133437.4:c.26436G>C