Canonical Allele Identifier: PA302492
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191971
ClinVar RCV Id: RCV000172340 RCV000219175 RCV000469863 RCV000626790 RCV001131408 RCV001134387 RCV001134389 RCV001134390 RCV001134388 RCV002390415 RCV003150042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp13841Asn
CA302489
NM_001267550.2:c.41521G>A