Canonical Allele Identifier: PA141478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47598
ClinVar RCV Id: RCV000040867 RCV000118794 RCV000248345 RCV000260558 RCV000264048 RCV000322722 RCV000354955 RCV000321435 RCV000361061 RCV001079943 RCV000768847 RCV002222153 RCV004534950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala32765Gly
CA141474
NM_001267550.2:c.98294C>G