Canonical Allele Identifier: PA645409392
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405095
ClinVar RCV Id: RCV000461969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn9377Lys
CA1999655
NM_001267550.2:c.28131C>A
CA349440246
NM_001267550.2:c.28131C>G