Canonical Allele Identifier: PA2826463881
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127627
ClinVar RCV Id: RCV000115496 RCV000212598 RCV000477595 RCV000663103 RCV001818271 RCV003997267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Phe328Leu
CA017419
NM_001258281.1:c.984T>G
CA346733829
NM_001258281.1:c.982T>C
CA346733839
NM_001258281.1:c.984T>A