Canonical Allele Identifier: PA2826465236
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786832
ClinVar RCV Id: RCV002432541 RCV003098673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu653Phe
CA346729336
NM_001258281.1:c.1959G>C
CA346729337
NM_001258281.1:c.1959G>T