Canonical Allele Identifier: PA916031229
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321371
ClinVar RCV Id: RCV000286700 RCV001094364 RCV002522903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ser119Cys
CA8253054
NM_001351830.2:c.356C>G