Canonical Allele Identifier: PA645383656
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332948
ClinVar RCV Id: RCV000267865 RCV000271336 RCV000297530 RCV000320627 RCV000358996 RCV000354761 RCV000413035 RCV001494675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Gly2386Ser
CA2004888
NM_133379.5:c.7156G>A