Canonical Allele Identifier: PA202120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196056
ClinVar RCV Id: RCV000176782 RCV000460701 RCV000620952 RCV001133987 RCV001082646 RCV001133986 RCV001133988 RCV001133989 RCV001133990 RCV001170572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser23128Tyr
CA202117
NM_001267550.2:c.69383C>A