Canonical Allele Identifier: PA141260
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47522
ClinVar RCV Id: RCV000040791 RCV000726970 RCV000643343 RCV001129835 RCV001129836 RCV001129837 RCV001129838 RCV001129839 RCV002362645 RCV003486608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr30778Arg
CA141256
NM_001267550.2:c.92333C>G