Canonical Allele Identifier: PA2826925896
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313220
ClinVar RCV Id: RCV000347988 RCV001786361 RCV001820930 RCV002487387 RCV004544558
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295062.1:p.Leu1517Phe
CA7169808
NM_001308133.2:c.4549C>T