Canonical Allele Identifier: PA141231
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47512
ClinVar RCV Id: RCV000040781 RCV000294400 RCV000307351 RCV000359863 RCV000347053 RCV000403395 RCV001081378 RCV000723853 RCV002362643 RCV003149661 RCV004541191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp30534Val
CA141227
NM_001267550.2:c.91601A>T