Canonical Allele Identifier: PA658800258
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 526352
ClinVar RCV Id: RCV000630873 RCV001256405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro1194Leu
CA397485658
NM_000135.4:c.3581C>T