Canonical Allele Identifier: PA916015101
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408171
ClinVar RCV Id: RCV000474793 RCV000499924 RCV000765324 RCV001579530 RCV003418176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Arg1144Trp
CA8251153
NM_001286167.3:c.3430C>T