Canonical Allele Identifier: PA2826423965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47442
ClinVar RCV Id: RCV000040711 RCV000247193 RCV000335949 RCV000305618 RCV000341787 RCV000406632 RCV000391984 RCV000477567 RCV000726282 RCV001170551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg26685Gln
CA141014
NM_001256850.1:c.80054G>A