Canonical Allele Identifier: PA2828034475
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353672
ClinVar RCV Id: RCV001863538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341847.1:p.Val1074Phe
CA374111793
NM_001354918.1:c.3220G>T