Canonical Allele Identifier: PA178542
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165860
ClinVar RCV Id: RCV000152232 RCV000457813 RCV000620418 RCV000768945 RCV000997409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile23368Val
CA178539
NM_001267550.2:c.70102A>G