Canonical Allele Identifier: PA2826926829
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 946874
ClinVar RCV Id: RCV001217827
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295063.1:p.Gln522Pro
CA389592721
NM_001308134.2:c.1565A>C