Canonical Allele Identifier: PA645397577
Gene: COL17A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 298691
ClinVar RCV Id: RCV000316322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000485.3:p.Asp1258Asn
CA5677810
NM_000494.4:c.3772G>A