Canonical Allele Identifier: PA916014744
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 134286
ClinVar RCV Id: RCV000120959 RCV000465739 RCV003237725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Met160Ile
CA159359
NM_001286167.3:c.480G>A
CA397480725
NM_001286167.3:c.480G>T
CA397480726
NM_001286167.3:c.480G>C