Canonical Allele Identifier: PA2826425142
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404848
ClinVar RCV Id: RCV000475196 RCV000726797 RCV001170308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg28624Trp
CA1987742
NM_001256850.1:c.85870C>T