ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA2826463840
Gene: MSH2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
449782
ClinVar RCV Id:
RCV000519754
RCV001010007
RCV000547472
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001245210.1:p.Pro319Ala
CA46702663
NM_001258281.1:c.955C>G