Canonical Allele Identifier: PA181656
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178175
ClinVar RCV Id: RCV000154900 RCV000201380 RCV000230724 RCV000621138 RCV000710279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile29658Val
CA181653
NM_001267550.2:c.88972A>G