Canonical Allele Identifier: PA202119
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_001243779.1:p.Ser21487Tyr
CA202117
NM_001256850.1:c.64460C>A