Canonical Allele Identifier: PA2830217804
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202794
ClinVar RCV Id: RCV000184727 RCV001129618 RCV001129619 RCV001129620 RCV001129621 RCV001129617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Leu12788Val
CA310310
NM_133432.3:c.38362C>G