Canonical Allele Identifier: PA141254
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47520
ClinVar RCV Id: RCV000040789 RCV000082448 RCV000247505 RCV000277773 RCV000290790 RCV000348133 RCV000387528 RCV000330728 RCV000380748 RCV000852789 RCV001083918 RCV001132527 RCV001132528 RCV001798198 RCV002227930 RCV003993770 RCV004534939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro29085Ser
CA141251
NM_001256850.1:c.87253C>T