Canonical Allele Identifier: PA2826427117
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535602
ClinVar RCV Id: RCV000643674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val31713Leu
CA349426853
NM_001256850.1:c.95137G>C
CA349426854
NM_001256850.1:c.95137G>T