Canonical Allele Identifier: PA141178
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47493
ClinVar RCV Id: RCV000040762 RCV000458878 RCV000733290 RCV003147329 RCV002362639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val27415Met
CA141176
NM_133378.4:c.82243G>A