Canonical Allele Identifier: PA645404192
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 321347
ClinVar RCV Id: RCV000350181 RCV000765328
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000126.2:p.Pro799Ser
CA8251735
NM_000135.4:c.2395C>T