Canonical Allele Identifier: PA2825497154
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353672
ClinVar RCV Id: RCV001863538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Val1125Phe
CA374111793
NM_001083603.3:c.3373G>T