Canonical Allele Identifier: PA2826924541
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313188
ClinVar RCV Id: RCV000291828 RCV000767964 RCV001820925 RCV002256201 RCV003224257 RCV004537773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Leu57Phe
CA7168711
NM_001308133.2:c.171G>C
CA389587256
NM_001308133.2:c.171G>T