Canonical Allele Identifier: PA181701
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96307
ClinVar RCV Id: RCV000082433 RCV000154913 RCV000229774 RCV000252341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser25442Pro
CA181698
NM_001256850.1:c.76324T>C