Canonical Allele Identifier: PA658661652
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 456256
ClinVar RCV Id: RCV000540275 RCV001090527 RCV002490947 RCV003994000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Ala60Glu
CA7168713
NM_020937.4:c.179C>A