Canonical Allele Identifier: PA283132
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46878
ClinVar RCV Id: RCV000040148 RCV000225853 RCV000245854 RCV000770065 RCV001135520 RCV001135521 RCV001130444 RCV001130445 RCV001135522 RCV004534893 RCV004546420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10917Leu
CA283129
NM_001267550.2:c.32750C>T