Canonical Allele Identifier: PA916014990
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456101
ClinVar RCV Id: RCV000542670 RCV001120360 RCV001562680 RCV003409764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Glu886Asp
CA8251602
NM_001286167.3:c.2658G>C
CA397438694
NM_001286167.3:c.2658G>T