Canonical Allele Identifier: PA2825507848
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Met971Val
CA374111821
NM_001083605.3:c.2911A>G