Canonical Allele Identifier: PA2830208014
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203055
ClinVar RCV Id: RCV000299494 RCV000369666 RCV000356693 RCV000524719 RCV000331220 RCV000390641 RCV000713946 RCV000764298 RCV000621440 RCV002282013 RCV001270048 RCV003486755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Trp30910Gly
CA311103
NM_133378.4:c.92728T>G