Canonical Allele Identifier: PA2741990059
Gene: SOST HGNC NCBI

Linked Data

ClinVar Variation Id: 2522680
ClinVar RCV Id: RCV003260690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079513.1:p.Ala199Ser
CA8592762
NM_025237.3:c.595G>T