Canonical Allele Identifier: PA2826633148
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142663
ClinVar RCV Id: RCV000132010 RCV000234247 RCV000412120 RCV000484116 RCV000708888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala849Gly
CA012948
NM_001281493.2:c.2546C>G