Canonical Allele Identifier: PA2825329033
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2711764
ClinVar RCV Id: RCV003524289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018122.1:p.Met116Leu
CA397481005
NM_001018112.2:c.346A>T
CA397481007
NM_001018112.2:c.346A>C