Canonical Allele Identifier: PA645409354
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238729
ClinVar RCV Id: RCV000230408 RCV000594931 RCV000727265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn9066Lys
CA1999851
NM_001267550.2:c.27198C>G
CA349456157
NM_001267550.2:c.27198C>A