Canonical Allele Identifier: PA916031234
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321370
ClinVar RCV Id: RCV000371929 RCV002522902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Ala129Val
CA8253042
NM_001351830.2:c.386C>T