Canonical Allele Identifier: PA2830212951
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 283986
ClinVar RCV Id: RCV000537307 RCV000513491 RCV000617967 RCV000770108 RCV002244732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn4183Ser
CA2002605
NM_133432.3:c.12548A>G