Canonical Allele Identifier: PA2579913009
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074504
ClinVar RCV Id: RCV004014038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn254Thr
CA346732380
NM_000251.3:c.761A>C