Canonical Allele Identifier: PA181859
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178232
ClinVar RCV Id: RCV000154967 RCV000464747 RCV000660516 RCV001130652 RCV000725082 RCV001130653 RCV000852883 RCV001129954 RCV001130654 RCV004534977
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile9264Val
CA181857
NM_001256850.1:c.27790A>G