Canonical Allele Identifier: PA2826587197
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428382
ClinVar RCV Id: RCV000491517 RCV000797850 RCV000759147 RCV003464057 RCV004003460 RCV003316642
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe1021Ser
CA46719891
NM_001281494.2:c.3062T>C