Canonical Allele Identifier: PA2826463395
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127654
ClinVar RCV Id: RCV000115544 RCV000472973 RCV000212593 RCV001193849 RCV000663090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp216Gly
CA022423
NM_001258281.1:c.647A>G