ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA355693
Gene: FANCC
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000127.2:p.Tyr430Ter
NM_000136.3:c.1290C>A
NM_000136.3:c.1290C>G