Allele Registry

Canonical Allele Identifier: PA145938

Gene: PTCH1 HGNC NCBI

ClinVar RCV:

RCV000008705

RCV000034564

RCV000078462

RCV000206005

RCV000568375

RCV002504769

ClinVar Variation:

8222

HGVS (amino-acid)	Matching Registered Transcripts
NP_001077071.1:p.Thr662Met	CA145935 NM_001083602.3:c.1985C>T