Canonical Allele Identifier: PA2826080705
Gene: MCFD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2870
ClinVar RCV Id: RCV000003004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164982.1:p.Asp110Glu
CA115788
NM_001171511.3:c.330C>G
CA346710541
NM_001171511.3:c.330C>A