Canonical Allele Identifier: PA2826463961
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127629
ClinVar RCV Id: RCV000115499 RCV000212601 RCV000515341 RCV000532709 RCV003467045 RCV003997269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln347Pro
CA017617
NM_001258281.1:c.1040A>C