Canonical Allele Identifier: PA302922
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196196
ClinVar RCV Id: RCV000375971 RCV000388603 RCV000464293 RCV000273519 RCV000617391 RCV000219446 RCV000316543 RCV000334102 RCV000725268 RCV003150052 RCV003319185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp32079Asn
CA302919
NM_001267550.2:c.96235G>A