Canonical Allele Identifier: PA295774
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 137839
ClinVar RCV Id: RCV000154988 RCV000266819 RCV000303282 RCV000306728 RCV000263263 RCV000357808 RCV000472153 RCV000769066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile6321Val
CA295771
NM_001267550.2:c.18961A>G