Canonical Allele Identifier: PA2826926634
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313196
ClinVar RCV Id: RCV000353097 RCV001706480 RCV002258875 RCV004544556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Glu309Ala
CA7168890
NM_001308134.2:c.926A>C