Canonical Allele Identifier: PA2830201848
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229543
ClinVar RCV Id: RCV000220841 RCV000304616 RCV000401224 RCV000301428 RCV000356180 RCV000340685 RCV000537936 RCV001171246 RCV001574925 RCV002365160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly28476Val
CA1987351
NM_133378.4:c.85427G>T