ClinGen Allele Registry
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Canonical Allele Identifier:
PA645402789
Gene: FANCC
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000127.2:p.Trp533Ter
NM_000136.3:c.1598G>A
NM_000136.3:c.1598_1599insAG
NM_000136.3:c.1599G>A