Canonical Allele Identifier: PA181987
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178271
ClinVar RCV Id: RCV000155012 RCV000643286 RCV001704127
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg1421Trp
CA181985
NM_001267550.2:c.4261C>T