Canonical Allele Identifier: PA178601
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165891
ClinVar RCV Id: RCV000152252 RCV000172283 RCV000298339 RCV000312931 RCV000353195 RCV000408391 RCV000404677 RCV000470625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21916Trp
CA178599
NM_001267550.2:c.65746C>T