Canonical Allele Identifier: PA645428852
Gene: C2orf42 HGNC NCBI

Linked Data

ClinVar Variation Id: 252715
ClinVar RCV Id: RCV000238669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060350.1:p.Pro176Leu
CA1697286
NM_017880.3:c.527C>T