ClinGen Allele Registry
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Canonical Allele Identifier:
PA645405112
Gene: FANCI
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000228956
RCV000482252
RCV000766508
RCV001094276
RCV003955318
ClinVar Variation:
238309
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001106849.1:p.Met525Val
CA7723058
NM_001113378.1:c.1573A>G