Canonical Allele Identifier: PA138774
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46618
ClinVar RCV Id: RCV000039888 RCV000172697 RCV000249224 RCV000660557 RCV000852909 RCV001131189 RCV001131186 RCV001131188 RCV001170649 RCV001081556 RCV001131187 RCV004534854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp4272Tyr
CA138772
NM_133378.4:c.12814G>T