Canonical Allele Identifier: PA139036
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_596869.4:p.Val6554Met
CA139034
NM_133378.4:c.19660G>A