Canonical Allele Identifier: PA2826002287
Gene: PYGM HGNC NCBI

Linked Data

ClinVar Variation Id: 878938
ClinVar RCV Id: RCV001105987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158188.1:p.Lys685Asn
CA381164659
NM_001164716.1:c.2055A>T
CA381164667
NM_001164716.1:c.2055A>C