Canonical Allele Identifier: PA310077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202718
ClinVar RCV Id: RCV000286006 RCV000228857 RCV000342179 RCV000307291 RCV000347210 RCV000287146 RCV000395829 RCV000725529 RCV000768991 RCV001262868 RCV002433826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala16625Ser
CA310076
NM_001256850.1:c.49873G>T