Canonical Allele Identifier: PA2826632226
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410500
ClinVar RCV Id: RCV000460082 RCV000580547 RCV004001849 RCV003463940 RCV004525934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala638Ser
CA069657
NM_001281493.2:c.1912G>T