Canonical Allele Identifier: PA2826463794
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127626
ClinVar RCV Id: RCV000115493 RCV000122979 RCV000580948 RCV003997266
ClinVar Variation Id: 842807
ClinVar RCV Id: RCV001045289 RCV001189516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln308His
CA017281
NM_001258281.1:c.924G>C
CA346733612
NM_001258281.1:c.924G>T