Canonical Allele Identifier: PA181829
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178221
ClinVar RCV Id: RCV000157561 RCV000154956 RCV000243216 RCV000852863 RCV001080889 RCV000724471 RCV001131898 RCV001798509 RCV001131899 RCV001132870 RCV001132871 RCV001132872 RCV004544426
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro13156Thr
CA181826
NM_001267550.2:c.39466C>A