Canonical Allele Identifier: PA140258
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47185
ClinVar RCV Id: RCV000040455 RCV000172650 RCV000263771 RCV000317683 RCV000246008 RCV000387122 RCV000292758 RCV000458325 RCV000318648 RCV003149651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr19217Ala
CA140255
NM_001256850.1:c.57649A>G