Canonical Allele Identifier: PA645431340
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313199
ClinVar RCV Id: RCV000383479 RCV000484209 RCV000763929 RCV001292951 RCV002255361 RCV004537776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Leu526Val
CA7169086
NM_020937.4:c.1576C>G