ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826463740
Gene: MSH2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
96016
ClinVar RCV:
RCV000574719
RCV000629732
RCV003997140
ClinVar Variation:
90541
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Asn295Ser
CA017221
NM_001258281.1:c.884A>G