ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA167938
Gene: MSH2
HGNC
NCBI
Linked Data
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_000242.1:p.Gln510His
NM_000251.3:c.1530G>C
NM_000251.3:c.1530G>T