Canonical Allele Identifier: PA311969
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_001243779.1:p.Ser6902Phe
CA311968
NM_001256850.1:c.20705C>T