Canonical Allele Identifier: PA1139677374
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_000242.1:p.Lys246Asn
CA346732238
NM_000251.3:c.738A>C
CA346732241
NM_000251.3:c.738A>T