Canonical Allele Identifier: PA2826416474
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263480
ClinVar RCV Id: RCV000244515 RCV000463022 RCV000598397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp13021Glu
CA1995783
NM_001256850.1:c.39063T>G
CA349646553
NM_001256850.1:c.39063T>A