Canonical Allele Identifier: PA916067010
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn9790Ser
CA1993349
NM_133437.4:c.29369A>G