Canonical Allele Identifier: PA159556
Gene: FANCE HGNC NCBI

Linked Data

ClinVar Variation Id: 134343
ClinVar RCV Id: RCV000121017 RCV000229190 RCV003153393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068741.1:p.Pro445Ser
CA159554
NM_021922.3:c.1333C>T