Canonical Allele Identifier: PA181934
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178256
ClinVar RCV Id: RCV000154996 RCV000725276 RCV001087743 RCV003486696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg4120His
CA181933
NM_133378.4:c.12359G>A