Canonical Allele Identifier: PA658660582
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 456164
ClinVar RCV Id: RCV000527037 RCV002051864 RCV002358436
ClinVar Variation Id: 2446385
ClinVar RCV Id: RCV003221315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Asp197Glu
CA374109706
NM_000136.3:c.591C>G
CA374109707
NM_000136.3:c.591C>A