Canonical Allele Identifier: PA2826710774
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134277
ClinVar RCV Id: RCV000120950 RCV000537860 RCV003144133 RCV003477509
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Ser103Leu
CA159334
NM_001286167.3:c.308C>T