Canonical Allele Identifier: PA2830202426
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 598297
ClinVar RCV Id: RCV000734656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly29668Glu
CA349445826
NM_133378.4:c.89003G>A