Canonical Allele Identifier: PA140635
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47309
ClinVar RCV Id: RCV000040579 RCV000172642 RCV001084590 RCV001133157 RCV001133159 RCV001133161 RCV001133158 RCV001133160 RCV002326758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala24046Val
CA140631
NM_001267550.2:c.72137C>T