Canonical Allele Identifier: CA974015996
Gene: PPL HGNC NCBI

Linked Data

dbSNP Id: rs2089421876
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.4951202C>A , CM000678.2:g.4951202C>A GRCh38
NC_000016.9:g.5001203C>A , CM000678.1:g.5001203C>A GRCh37
NC_000016.8:g.4941204C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000592772.1:c.-92+9362G>T ENSP00000467699.1:n.-92+9362G>T
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