Canonical Allele Identifier: PA2826463634
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220628
ClinVar RCV Id: RCV000663023 RCV001320681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly272Ala
CA349698
NM_001258281.1:c.815G>C