Canonical Allele Identifier: PA2826423471
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47411
ClinVar RCV Id: RCV000040681 RCV000300172 RCV000322064 RCV000353764 RCV000456607 RCV000768905 RCV000357436 RCV000997376 RCV002345318 RCV000787943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys25827Gln
CA140922
NM_001256850.1:c.77479A>C