Canonical Allele Identifier: PA645485952
Gene: MEGF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235520
ClinVar RCV Id: RCV000224648 RCV001082590 RCV002516229 RCV003919907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001401.2:p.Pro2491Leu
CA9476230
NM_001410.3:c.7472C>T