Canonical Allele Identifier: PA2825205358
Gene: GNAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2627910
ClinVar RCV Id: RCV003389351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000507.1:p.Phe273Leu
CA409452751
NM_000516.7:c.817T>C
CA409452758
NM_000516.7:c.819C>A
CA409452760
NM_000516.7:c.819C>G