Canonical Allele Identifier: PA2830211549
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192073
ClinVar RCV Id: RCV000172464 RCV000642748 RCV002362887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Asn2263Lys
CA238249
NM_133432.3:c.6789T>A
CA349681409
NM_133432.3:c.6789T>G