Canonical Allele Identifier: PA311952
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203295
ClinVar RCV Id: RCV000220902 RCV000643152 RCV001721182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met6794Thr
CA311951
NM_001256850.1:c.20381T>C