Canonical Allele Identifier: PA311908
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203281
ClinVar RCV Id: RCV000220599 RCV000469447 RCV000852898 RCV004537570 RCV003137756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr6324Asn
CA311907
NM_001256850.1:c.18971C>A