Canonical Allele Identifier: CA12141737
Gene: PART1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs26949

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529473T>C , CM000667.2:g.60529473T>C GRCh38
NC_000005.9:g.59825300T>C , CM000667.1:g.59825300T>C GRCh37
NC_000005.8:g.59861057T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.781T>C