Canonical Allele Identifier: PA115794
Gene: MCFD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2870
ClinVar RCV Id: RCV000003004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164979.1:p.Asp129Glu
CA115788
NM_001171508.2:c.387C>G
CA346710541
NM_001171508.2:c.387C>A