Canonical Allele Identifier: PA916011914
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142663
ClinVar RCV Id: RCV000132010 RCV000234247 RCV000412120 RCV000484116 RCV000708888
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ala849Gly
CA012948
NM_001281494.2:c.2546C>G