Allele Registry

Canonical Allele Identifier: PA645397555

Gene: COL17A1 HGNC NCBI

ClinVar RCV:

RCV000427953

ClinVar Variation:

390382

HGVS (amino-acid)	Matching Registered Transcripts
NP_000485.3:p.Gly636Arg	CA5678815 NM_000494.4:c.1906G>C CA16605963 NM_000494.4:c.1906G>A