Canonical Allele Identifier: PA2825493075
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Met362Thr
CA374119501
NM_001083603.3:c.1085T>C