Canonical Allele Identifier: PA2741865530
Gene: FANCA HGNC NCBI

Linked Data

ClinVar Variation Id: 2711764
ClinVar RCV Id: RCV003524289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338759.1:p.Met116Leu
CA397481005
NM_001351830.2:c.346A>T
CA397481007
NM_001351830.2:c.346A>C