Canonical Allele Identifier: PA2826421189
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467426
ClinVar RCV Id: RCV000547446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro21733Ala
CA349664840
NM_001256850.1:c.65197C>G