Canonical Allele Identifier: PA658661207
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 456101
ClinVar RCV Id: RCV000542670 RCV001120360 RCV001562680 RCV003409764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Glu886Asp
CA8251602
NM_000135.4:c.2658G>C
CA397438694
NM_000135.4:c.2658G>T