Canonical Allele Identifier: PA2825507822
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351084
ClinVar RCV Id: RCV002051477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Lys960Arg
CA374111884
NM_001083605.3:c.2879A>G