Canonical Allele Identifier: PA2825502793
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077073.1:p.Met652Thr
CA374114313
NM_001083604.3:c.1955T>C