Canonical Allele Identifier: PA2573203657
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1369364
ClinVar RCV Id: RCV001870590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Cys125Ser
CA397480951
NM_001351830.2:c.374G>C
CA397480953
NM_001351830.2:c.373T>A