Canonical Allele Identifier: PA2826635781
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 923297
ClinVar RCV Id: RCV001183872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp411Glu
CA346751066
NM_001281494.2:c.1233T>A
CA346751067
NM_001281494.2:c.1233T>G