Canonical Allele Identifier: PA916066496
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp8542Asn
CA139896
NM_133437.4:c.25624G>A