Canonical Allele Identifier: PA2826414442
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_001243779.1:p.Asn8749Lys
CA1999851
NM_001256850.1:c.26247C>G
CA349456157
NM_001256850.1:c.26247C>A