Canonical Allele Identifier: PA311970
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203300
ClinVar RCV Id: RCV000213535 RCV000251604 RCV000296518 RCV000335093 RCV000338709 RCV000401816 RCV000406874 RCV000470210 RCV000725490 RCV000770079
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser7219Phe
CA311968
NM_001267550.2:c.21656C>T