Canonical Allele Identifier: PA139045
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46721
ClinVar RCV Id: RCV000039991 RCV000082372 RCV000293069 RCV000390050 RCV000335014 RCV000352590 RCV000406710 RCV000852891 RCV001082941 RCV001798135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe7529Leu
CA139042
NM_001256850.1:c.22587C>G
CA349508808
NM_001256850.1:c.22587C>A
CA349508841
NM_001256850.1:c.22585T>C