Canonical Allele Identifier: PA2826413812
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46719
ClinVar RCV Id: RCV000039989 RCV000726274 RCV001130096 RCV001135129 RCV001135131 RCV001135128 RCV001135130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val7481Met
CA139034
NM_001256850.1:c.22441G>A