Canonical Allele Identifier: PA2830196680
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_596869.4:p.Asn16312Lys
CA1993218
NM_133378.4:c.48936C>A
CA349528489
NM_133378.4:c.48936C>G