Canonical Allele Identifier: PA2830300908
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1505824
ClinVar RCV Id: RCV001999610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_690610.1:p.Asn243Lys
CA377509821
NM_152871.4:c.729T>A
CA377509822
NM_152871.4:c.729T>G