Canonical Allele Identifier: PA2826419120
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404856
ClinVar RCV Id: RCV000460883 RCV000591455 RCV002323680 RCV003330687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu18016Asp
CA1992749
NM_001256850.1:c.54048A>C
CA349500202
NM_001256850.1:c.54048A>T