Canonical Allele Identifier: PA2826428469
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2946440
ClinVar RCV Id: RCV003806726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala33192Gly
CA349411542
NM_001256850.1:c.99575C>G