Canonical Allele Identifier: PA2826490022
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332887
ClinVar RCV Id: RCV000281197 RCV000296455 RCV000335141 RCV000338547 RCV000388328 RCV000466619 RCV000598451 RCV001534640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg10985Pro
CA1998485
NM_001267550.2:c.32954G>C