Canonical Allele Identifier: PA302513
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192021
ClinVar RCV Id: RCV000172398 RCV000306811 RCV000346409 RCV000303063 RCV000342923 RCV000401694 RCV000464696 RCV001170094 RCV004535176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys6199Met
CA302511
NM_001256850.1:c.18596A>T