Canonical Allele Identifier: PA916015055
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 408176
ClinVar RCV Id: RCV000469035 RCV001274568 RCV001573434 RCV003424019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asp1033Glu
CA8251332
NM_001286167.3:c.3099C>A
CA397486696
NM_001286167.3:c.3099C>G