Canonical Allele Identifier: PA2499287203
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 1044073
ClinVar RCV Id: RCV001348272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065988.1:p.Met396Leu
CA7168967
NM_020937.4:c.1186A>C
CA389591092
NM_020937.4:c.1186A>T