Canonical Allele Identifier: PA2826463269
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408527
ClinVar RCV Id: RCV000568397 RCV000467943 RCV001171949 RCV003335335 RCV004000790
ClinVar Variation Id: 2584100
ClinVar RCV Id: RCV003335548
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Met187Ile
CA16610795
NM_001258281.1:c.561G>A
CA346732367
NM_001258281.1:c.561G>C
CA346732369
NM_001258281.1:c.561G>T