Canonical Allele Identifier: PA2826925179
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456253
ClinVar RCV Id: RCV000526327 RCV001591192 RCV003316678 RCV002257786 RCV004541643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Arg730His
CA7169305
NM_001308133.2:c.2189G>A