Canonical Allele Identifier: PA915963544
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 822603
ClinVar RCV Id: RCV001018086 RCV002549471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ser287Asn
CA346740589
NM_000179.3:c.860G>A