Canonical Allele Identifier: PA311069
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203043
ClinVar RCV Id: RCV000185056 RCV000303989 RCV000298988 RCV000335265 RCV000392376 RCV000358712 RCV001704935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser32987Pro
CA311067
NM_001267550.2:c.98959T>C