ClinGen Allele Registry
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Canonical Allele Identifier:
PA299487
Gene: MSH6
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
180096
ClinVar RCV:
RCV000160697
RCV000226708
RCV000564770
RCV000663071
RCV001175454
RCV003467253
RCV003998504
ClinVar Variation:
182648
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000170.1:p.Asn1229Ser
CA013811
NM_000179.3:c.3686A>G