Canonical Allele Identifier: PA309080
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202321
ClinVar RCV Id: RCV000184160 RCV001852382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val20905Met
CA309079
NM_001256850.1:c.62713G>A