Canonical Allele Identifier: PA2826420717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 220680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser20894Asn
CA348224
NM_001256850.1:c.62681G>A