Canonical Allele Identifier: PA141255
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro30726Ser
CA141251
NM_001267550.2:c.92176C>T