Canonical Allele Identifier: PA2826463281
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231904
ClinVar RCV Id: RCV000222095 RCV000526634 RCV000757937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser189Gly
CA040330
NM_001258281.1:c.565A>G