Canonical Allele Identifier: PA2826420647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47249
ClinVar RCV Id: RCV000040519 RCV000618423 RCV000462522 RCV001507592 RCV003989305
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly20742Arg
CA140455
NM_001256850.1:c.62224G>A
CA349424385
NM_001256850.1:c.62224G>C