Canonical Allele Identifier: PA2826414611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1030139
ClinVar RCV Id: RCV001331624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro9061Ser
CA60964328
NM_001256850.1:c.27181C>T