Canonical Allele Identifier: PA302885
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196065
ClinVar RCV Id: RCV000265766 RCV000300684 RCV000337171 RCV000361406 RCV000397204 RCV000725272 RCV001081316 RCV002326968 RCV002227452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn24256Asp
CA302882
NM_001267550.2:c.72766A>G