Canonical Allele Identifier: PA2827456398
Gene: C2orf42 HGNC NCBI

Linked Data

ClinVar Variation Id: 252715
ClinVar RCV Id: RCV000238669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335688.1:p.Pro176Leu
CA1697286
NM_001348759.2:c.527C>T