Canonical Allele Identifier: PA916065647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47006
ClinVar RCV Id: RCV000040276 RCV000287419 RCV000272075 RCV000322491 RCV000342339 RCV000377170 RCV000470629 RCV000617450 RCV001719770 RCV004534900
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala6754Val
CA139743
NM_133437.4:c.20261C>T