Canonical Allele Identifier: PA1139737316
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 945326
ClinVar RCV Id: RCV001215944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Arg422Cys
CA7168979
NM_020937.4:c.1264C>T