Canonical Allele Identifier: PA2826926517
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 313193
ClinVar RCV Id: RCV000338024 RCV000503452 RCV001293001 RCV001706479 RCV004537775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Thr176Ile
CA7168797
NM_001308134.2:c.527C>T