Canonical Allele Identifier: PA2830209342
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 863553
ClinVar RCV Id: RCV001070546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32876Ser
CA349406040
NM_133378.4:c.98627C>G
CA349406045
NM_133378.4:c.98626A>T