Canonical Allele Identifier: PA2826465153
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 923587
ClinVar RCV Id: RCV001184412 RCV003759014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser633Thr
CA346729225
NM_001258281.1:c.1897T>A