Canonical Allele Identifier: PA2826462885
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682011
ClinVar RCV Id: RCV003477303 RCV003759883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu53Phe
CA346730125
NM_001258281.1:c.159G>C
CA346730127
NM_001258281.1:c.159G>T