Canonical Allele Identifier: PA311875
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203270
ClinVar RCV Id: RCV000215380 RCV000253515 RCV000726101 RCV001079996 RCV001798658 RCV004537568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys5810Gly
CA311874
NM_001256850.1:c.17428T>G