Canonical Allele Identifier: PA178816
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166005
ClinVar RCV Id: RCV000152339 RCV000172664 RCV000276790 RCV000328242 RCV000331815 RCV000382730 RCV000367766 RCV000622012 RCV001086129 RCV001837462 RCV004544373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg16905His
CA178813
NM_001267550.2:c.50714G>A