Canonical Allele Identifier: PA299487
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182648
ClinVar RCV Id: RCV000160697 RCV000226708 RCV000564770 RCV000663071 RCV001175454 RCV003467253 RCV003998504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn1229Ser
CA013811
NM_000179.3:c.3686A>G