Canonical Allele Identifier: PA179198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166293
ClinVar RCV Id: RCV000152478 RCV000540226 RCV001293078 RCV001719943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr3295Met
CA179196
NM_001256850.1:c.9884C>T