Canonical Allele Identifier: PA2830238637
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47464
ClinVar RCV Id: RCV000040733 RCV000172625 RCV000618830 RCV001086492 RCV001129292 RCV001129291 RCV001131993 RCV001131994 RCV001131995 RCV001293177 RCV001798189 RCV002227443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro20265Thr
CA141084
NM_133437.4:c.60793C>A