Canonical Allele Identifier: PA2830300856
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134375
ClinVar RCV Id: RCV000121049
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Asn231Lys
CA159640
NM_152871.4:c.693T>G
CA377509726
NM_152871.4:c.693T>A