Canonical Allele Identifier: PA238476
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192151
ClinVar RCV Id: RCV000172631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn26567Asp
CA238474
NM_001267550.2:c.79699A>G