Canonical Allele Identifier: PA181558
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178152
ClinVar RCV Id: RCV000154868 RCV001136023 RCV001136025 RCV001136024 RCV001136021 RCV001136022 RCV002415661 RCV004534966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Leu33058Val
CA181557
NM_133378.4:c.99172T>G