Canonical Allele Identifier: PA2828034455
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1950217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Met1070Thr
CA374111817
NM_001354918.1:c.3209T>C