Canonical Allele Identifier: PA2826416100
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467137
ClinVar RCV Id: RCV000539660 RCV000609462 RCV003139794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala12274Val
CA1996214
NM_001256850.1:c.36821C>T