Canonical Allele Identifier: PA2825510871
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2846490
ClinVar RCV Id: RCV003608856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Thr982Pro
CA374111754
NM_001083606.3:c.2944A>C