Canonical Allele Identifier: PA302582
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192090
ClinVar RCV Id: RCV000172483 RCV000412679 RCV000536793 RCV001129769 RCV001129770 RCV001129771 RCV001129768 RCV001129767 RCV003486722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala1081Ser
CA302579
NM_001267550.2:c.3241G>T