Canonical Allele Identifier: PA915982176
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332900
ClinVar RCV Id: RCV000276929 RCV000311952 RCV000329536 RCV000369112 RCV000368944 RCV001552864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro9760Leu
CA1999202
NM_001256850.1:c.29279C>T