Canonical Allele Identifier: PA141769
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47717
ClinVar RCV Id: RCV000040986 RCV000620414 RCV000726670 RCV000538774 RCV001131607 RCV001131608 RCV001131609 RCV001131610 RCV001131606 RCV001171217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35652Gln
CA141765
NM_001267550.2:c.106955G>A