Canonical Allele Identifier: PA2826465659
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455565
ClinVar RCV Id: RCV000550167 RCV000567964 RCV003459179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn769Ser
CA036330
NM_001258281.1:c.2306A>G