ClinGen Allele Registry
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Canonical Allele Identifier:
PA915984348
Gene: MSH2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
185977
ClinVar RCV:
RCV000167977
RCV000223301
RCV000240465
RCV003454423
ClinVar Variation:
188119
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Gly98Glu
CA021218
NM_001258281.1:c.293G>A