Canonical Allele Identifier: PA916052584
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 654746
ClinVar RCV Id: RCV000810761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Met480Ile
CA259618711
NM_020937.4:c.1440G>C
CA389592448
NM_020937.4:c.1440G>A
CA389592449
NM_020937.4:c.1440G>T