Canonical Allele Identifier: PA2830212140
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47578
ClinVar RCV Id: RCV000040847 RCV000082457 RCV001084542 RCV001133642 RCV001133644 RCV001133643 RCV001133640 RCV001133641 RCV004534948 RCV002444495 RCV003486612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ala2934Thr
CA141401
NM_133432.3:c.8800G>A