Canonical Allele Identifier: PA1139687012
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 855510
ClinVar RCV Id: RCV001060791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Glu1385Asp
CA397484276
NM_001286167.3:c.4155G>T
CA397484277
NM_001286167.3:c.4155G>C