Canonical Allele Identifier: PA916014958
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321347
ClinVar RCV Id: RCV000350181 RCV000765328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Pro799Ser
CA8251735
NM_001286167.3:c.2395C>T