Canonical Allele Identifier: PA2826418691
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238802
ClinVar RCV Id: RCV000229617 RCV002433965 RCV003137841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn17239Lys
CA1993218
NM_001256850.1:c.51717C>A
CA349528489
NM_001256850.1:c.51717C>G