Canonical Allele Identifier: PA645417701
Gene: SPTA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 293029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003117.2:p.Asp606Gly
CA1183620
NM_003126.2:c.1817A>G