Canonical Allele Identifier: PA2826926175
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 408221
ClinVar RCV Id: RCV000465642 RCV000765164 RCV000709952 RCV002255393 RCV001662428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Val1831Met
CA7170021
NM_001308133.2:c.5491G>A