Canonical Allele Identifier: PA2826710833
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1369364
ClinVar RCV Id: RCV001870590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Cys125Ser
CA397480951
NM_001286167.3:c.374G>C
CA397480953
NM_001286167.3:c.373T>A