Canonical Allele Identifier: PA916065618
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332859
ClinVar RCV Id: RCV000287871 RCV000295969 RCV000351115 RCV000385804 RCV000407698 RCV000869607 RCV003137953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala6622Thr
CA1995229
NM_133437.4:c.19864G>A