Canonical Allele Identifier: PA2826428977
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2437933
ClinVar RCV Id: RCV003137099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn33707Ser
CA349407156
NM_001256850.1:c.101120A>G