Canonical Allele Identifier: PA916015021
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456104
ClinVar RCV Id: RCV000555471 RCV001821477 RCV002254702 RCV003478120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Gln952His
CA8251452
NM_001286167.3:c.2856G>C
CA397431598
NM_001286167.3:c.2856G>T