Canonical Allele Identifier: PA2826714554
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1000018
ClinVar RCV Id: RCV001296091 RCV003992490 RCV003382501 RCV004036022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Asn1398Asp
CA397483690
NM_001286167.3:c.4192A>G