Canonical Allele Identifier: PA2580138067
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730347
ClinVar RCV Id: RCV002326523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Asn961Ser
CA374111876
NM_001083607.3:c.2882A>G