Canonical Allele Identifier: PA645378248
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237135
ClinVar RCV Id: RCV000233115 RCV000773125 RCV003320618 RCV003998708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala49Val
CA067716
NM_000179.3:c.146C>T