Canonical Allele Identifier: PA658660452
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 449791
ClinVar RCV Id: RCV000518936 RCV000692581 RCV001276468 RCV002384005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Gln3His
CA5137852
NM_000136.3:c.9A>T
CA374340535
NM_000136.3:c.9A>C