Canonical Allele Identifier: PA658800292
Gene: FANCC HGNC NCBI

Linked Data

ClinVar Variation Id: 526382
ClinVar RCV Id: RCV000630906 RCV003162794 RCV003238790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000127.2:p.Met16Leu
CA374340454
NM_000136.3:c.46A>T
CA374340458
NM_000136.3:c.46A>C