Canonical Allele Identifier: PA2826632755
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142482
ClinVar RCV Id: RCV000131620 RCV003758697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala762Thr
CA011817
NM_001281493.2:c.2284G>A