Canonical Allele Identifier: PA2826426398
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_001243779.1:p.Gly30595Glu
CA349445826
NM_001256850.1:c.91784G>A