Canonical Allele Identifier: PA139032
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46717
ClinVar RCV Id: RCV000039987 RCV000154089 RCV000270207 RCV000249580 RCV000299836 RCV000305761 RCV000402503 RCV000359255 RCV001081260 RCV001171039 RCV001358669 RCV004534871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp7451Asn
CA139029
NM_001256850.1:c.22351G>A