Canonical Allele Identifier: PA2826710805
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2711764
ClinVar RCV Id: RCV003524289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273096.1:p.Met116Leu
CA397481005
NM_001286167.3:c.346A>T
CA397481007
NM_001286167.3:c.346A>C