Canonical Allele Identifier: PA645409114
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282786
ClinVar RCV Id: RCV000270267 RCV000527307 RCV000725143 RCV001131793 RCV001131794 RCV001131796 RCV001131795 RCV001131797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn6931Ser
CA2001156
NM_001267550.2:c.20792A>G