Canonical Allele Identifier: PA916014913
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 265136
ClinVar RCV Id: RCV000255908 RCV000475267 RCV000989672 RCV001800637 RCV003920022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Cys625Ser
CA8251994
NM_001286167.3:c.1874G>C
CA397451864
NM_001286167.3:c.1873T>A