Canonical Allele Identifier: PA2826464987
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927535
ClinVar RCV Id: RCV001190855
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met597Leu
CA032288
NM_001258281.1:c.1789A>T
CA346728896
NM_001258281.1:c.1789A>C