Canonical Allele Identifier: PA916015104
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 435126
ClinVar RCV Id: RCV000503023 RCV000630890 RCV003478070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Thr1161Met
CA8251139
NM_001286167.3:c.3482C>T