Canonical Allele Identifier: PA915984014
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231062
ClinVar RCV Id: RCV000221016 RCV000702606 RCV003469023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala41Gly
CA10577932
NM_001258281.1:c.122C>G