Canonical Allele Identifier: PA2826462731
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134841
ClinVar RCV Id: RCV000121558 RCV000771511 RCV004528832 RCV000808087 RCV003997347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala4Thr
CA019989
NM_001258281.1:c.10G>A