Canonical Allele Identifier: PA2826463242
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 947813
ClinVar RCV Id: RCV001218951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys180Asn
CA346732238
NM_001258281.1:c.540A>C
CA346732241
NM_001258281.1:c.540A>T