Canonical Allele Identifier: PA2825085009
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023383
ClinVar RCV Id: RCV001323413 RCV002366192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala23Ser
CA346734779
NM_000179.3:c.67G>T