Canonical Allele Identifier: PA141567
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47636
ClinVar RCV Id: RCV000040905 RCV000082466 RCV000247307 RCV000282222 RCV000286768 RCV000371851 RCV000317271 RCV000341793 RCV000852925 RCV001084199 RCV000769103 RCV004534955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3120Gln
CA141561
NM_133379.5:c.9359G>A