Canonical Allele Identifier: PA916031213
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 237036
ClinVar RCV Id: RCV000231985 RCV001092318 RCV001094448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ser53Arg
CA8253156
NM_001351830.2:c.157A>C
CA397483313
NM_001351830.2:c.159C>A
CA397483314
NM_001351830.2:c.159C>G