Canonical Allele Identifier: PA141016
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47442
ClinVar RCV Id: RCV000040711 RCV000247193 RCV000335949 RCV000305618 RCV000341787 RCV000406632 RCV000391984 RCV000477567 RCV000726282 RCV001170551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg25758Gln
CA141014
NM_133378.4:c.77273G>A