Canonical Allele Identifier: PA916065591
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467172
ClinVar RCV Id: RCV000531429
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro6517Leu
CA60993148
NM_133437.4:c.19550C>T