Canonical Allele Identifier: PA645471999
Gene: EMD HGNC NCBI

Linked Data

ClinVar Variation Id: 435058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000108.1:p.Pro77Ser
CA415257679
NM_000117.3:c.229C>T