Canonical Allele Identifier: PA2826465082
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171156
ClinVar RCV Id: RCV001524078 RCV001872015
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile619Leu
CA346729149
NM_001258281.1:c.1855A>C
CA346729150
NM_001258281.1:c.1855A>T