Canonical Allele Identifier: PA2825490458
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077071.1:p.Leu1069Pro
CA374111741
NM_001083602.3:c.3206T>C