Canonical Allele Identifier: PA302429
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191870
ClinVar RCV Id: RCV000172223 RCV000302023 RCV000271594 RCV000277611 RCV000308136 RCV000346588 RCV000362784 RCV001170553 RCV001082315 RCV002354439 RCV004539586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg28291Cys
CA302426
NM_001267550.2:c.84871C>T