Canonical Allele Identifier: PA140698
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47328
ClinVar RCV Id: RCV000040598 RCV000534367 RCV000621675 RCV000724394 RCV000852812 RCV001293173 RCV003486596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn22275Asp
CA140696
NM_133378.4:c.66823A>G