Canonical Allele Identifier: PA1139684985
Gene: COL17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 879942
ClinVar RCV Id: RCV001107864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000485.3:p.Gly1319Ser
CA5677752
NM_000494.4:c.3955G>A