Canonical Allele Identifier: PA2830204027
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2946440
ClinVar RCV Id: RCV003806726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala32265Gly
CA349411542
NM_133378.4:c.96794C>G