Canonical Allele Identifier: PA2826465682
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 821417
ClinVar RCV Id: RCV001015809 RCV003320782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile775Leu
CA346730750
NM_001258281.1:c.2323A>C
CA346730753
NM_001258281.1:c.2323A>T