Canonical Allele Identifier: PA295534
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137798
ClinVar RCV Id: RCV000152272 RCV000229206 RCV000274784 RCV000314825 RCV000356882 RCV000401386 RCV000369478 RCV000619018 RCV001812061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val18081Ala
CA295532
NM_001256850.1:c.54242T>C