Canonical Allele Identifier: PA2829439868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47404
ClinVar RCV Id: RCV000040674 RCV000176835 RCV000227596 RCV000415094 RCV000619262 RCV000768910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg18235His
CA140899
NM_003319.4:c.54704G>A