Canonical Allele Identifier: PA2829443844
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47621
ClinVar RCV Id: RCV000040890 RCV000242155 RCV000206544 RCV000301140 RCV000297253 RCV000354426 RCV000367561 RCV000390707 RCV000390934 RCV000725311 RCV004534953 RCV001798207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Glu24236Lys
CA141530
NM_003319.4:c.72706G>A