Canonical Allele Identifier: PA658800262
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526331
ClinVar RCV Id: RCV000630847 RCV001121953 RCV003237964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1213Ala
CA8251038
NM_000135.4:c.3637C>G