Canonical Allele Identifier: PA139121
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46752
ClinVar RCV Id: RCV000040022 RCV000118744 RCV001087646 RCV004541139
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala8046Ser
CA139118
NM_001256850.1:c.24136G>T